METHOD FOR THE ENZYMATIC PRODUCTION OF BUTADIENE

Abstract

Described is a method for the enzymatic production of butadiene which allows to produce butadiene from crotyl alcohol. Also described are enzyme combinations and compositions containing such enzyme combinations which allow the enzymatic conversion of crotyl alcohol into butadiene. Furthermore, the invention relates to microorganisms which have been genetically modified so as to be able to produce butadiene from crotyl alcohol. Moreover, the invention relates to a method for the enzymatic production of crotyl alcohol from crotonyl-Coenzyme A. The obtained crotyl alcohol can be further converted into butadiene as described herein. Also described are enzyme combinations which allow to convert crotonyl-Coenzyme A into crotyl alcohol as well as (micro)organisms which express such enzyme combinations.

Description

The present invention relates to a method for the enzymatic production of butadiene which allows to produce butadiene from crotyl alcohol. The present invention also relates to microorganisms which have been genetically modified so as to produce butadiene.

The present invention also relates to a method for the enzymatic production of crotyl alcohol from crotonyl-Coenzyme A. The obtained crotyl alcohol can be further converted into butadiene as described herein. The present invention furthermore relates to enzyme combinations which allow to convert crotonyl-Coenzyme A into crotyl alcohol as well as to (micro)organisms which express such enzyme combinations.

Butadiene (1,3-butadiene) is a conjugated diene with the formula C₄H₆ (see FIG. 4). It is an important industrial chemical used as a monomer in the production of synthetic rubber. There exist different possibilities to produce butadiene. Butadiene is, for example, produced as a by product of the steam cracking process used to produce ethylene and other olefins. In this process butadiene occurs in the C4 stream and is normally isolated from other byproducts by extraction into a polar aprotic solvent, such as acetonitrile, from which it is then stripped. Butadiene can also be produced by the catalytic dehydrogenation of normal butane or it can be produced from ethanol. In the latter case, two different processes are in use. In a single-step process, ethanol is converted to butadiene, hydrogen and water at 400-450° C. over a metal oxide catalyst (Kirshenbaum, I. (1978), Butadiene. In M. Grayson (Ed.), Encyclopedia of Chemical Technology, 3rd ed., vol. 4, pp. 313-337. New York: John Wiley & Sons). In a two-step process, ethanol is oxidized to acetaldehyde which reacts with additional ethanol over a tantalum-promoted porous silica catalyst at 325-350° C. to yield butadiene (Kirshenbaum, I. (1978), loc cit.). Butadiene can also be produced by catalytic dehydrogenation of normal butenes.

For the past two decades, genetic engineering technologies have made possible the modification of the metabolism of micro-organisms, and hence their use to produce key substances which they would otherwise produce at a low yield. By enhancing naturally occurring metabolic pathways, these technologies open up new ways to bio-produce numerous compounds of industrial relevance. Several industrial compounds such as amino-acids for animal feed, biodegradable plastics or textile fibres are now routinely produced using genetically modified organisms. There are however no bio-processes using micro-organisms in place for the production of the major petrochemically derived molecules, in particular butadiene, since no micro-organisms are known as natural producers of butadiene even in small quantities. Given the large amounts of rubber produced worldwide and the increasing environmental concerns and the limited resources for producing butadiene using chemical processes, there is a need to provide alternative, environmentally-friendly and sustainable processes for the production of butadiene.

The present invention addresses this need and provides for the first time a process by which butadiene can be produced enzymatically starting from crotyl alcohol. Crotyl alcohol itself can be provided by the enzymatic conversion of crotonyl CoA which, in turn, can be provided starting from the metabolic intermediate acetyl-Coenzyme A (in the following acetyl-CoA) as described herein.

Thus, in a first aspect, the present invention relates to a process for the production of butadiene in which butadiene is produced by the enzymatic conversion of crotyl alcohol. Crotyl alcohol, also referred to as crotonyl alcohol or crotonol, is an unsaturated alcohol of formula C₄H₈O (see FIG. 1). Another name for crotyl alcohol is But-2-en-1-ol. It can be produced by reduction of crotonaldehyde (see FIG. 3). According to the present invention crotyl alcohol can be converted into butadiene by enzymatic reactions involving as intermediates crotyl phosphate and/or crotyl diphosphate. Thus, the principle underlying the present invention is that crotyl alcohol is first enzymatically activated by the conversion into crotyl phosphate or crotyl diphosphate and is then further converted into butadiene by the use of appropriate enzymes as described below.

Thus, the present invention relates, in a first aspect, to a method for the production of butadiene comprising the enzymatic conversion of crotyl alcohol into butadiene via crotyl phosphate or crotyl diphosphate.

The enzymatic conversion of crotyl alcohol into butadiene can occur via different alternative routes. In a first aspect (A), the present invention relates to a method for the production of butadiene comprising the enzymatic conversion of crotyl alcohol into butadiene via crotyl phosphate wherein said method comprises the steps of

(i) enzymatically converting crotyl alcohol into crotyl phosphate; and
(ii) enzymatically converting crotyl phosphate into butadiene.

This alternative is in the following referred to as Alternative A and the different steps are referred to as A(i) and A(ii).

As regards step A(i), the enzymatic conversion of crotyl alcohol into crotyl phosphate is a phosphorylation step and can be achieved by enzymes which catalyze the transfer of a phospho group onto a molecule, such as kinases. For example, enzymes which can be employed in this reaction are enzymes which are classified as E.C. 2.7.1, i.e. phosphotransferases with an alcohol group as acceptor, preferably enzymes which are classified as 2.7.1.50 (hydroxyethylthiazole kinase) or which are classified as E.C. 2.7.1.89 (thiamine kinase). Preferably, ATP is the donor of the phospho group in such a reaction. Thus, in one embodiment the enzymatic conversion of crotyl alcohol into crotyl phosphate can, e.g., be achieved by the use of a hydroxyethylthiazole kinase (EC 2.7.1.50). Hydroxyethylthiazole kinase is an enzyme which catalyzes the following reaction

ATP+4-methyl-5-(2-hydroxyethyl)thiazoleADP+4-methyl-5-(2-phosphoethyl)thiazole

The occurrence of this enzyme has been described for several organisms, e.g. for E. coli, Bacillus subtilis, Rhizobium leguminosarum, Pyrococcus horikoshii OT3, Saccharomyces cerevisiae.

In another embodiment the enzymatic conversion of crotyl alcohol into crotyl phosphate can, e.g., be achieved by the use of a thiamine kinase (EC 2.7.1.89). Thiamine kinase is an enzyme which catalyzes the following reaction

ATP+thiamineADP+thiamine phosphate

The occurrence of this enzyme has been described for several organisms, e.g. for E. coli and Salmonella enterica.

Hydroxyethylthiazole is a moiety of thiamine and shares with crotyl alcohol the following common structural motif CH—C—CH—CH₂—OH.

Thus, the inventor considers that a hydroxyethylthiazole kinase or a thiamine kinase could also act on other substrates which contain this motif and found that, indeed, different tested hydroxyethylthiazole kinases and thiamine kinases were capable of using crotyl alcohol as a substrate and converting it into crotyl phosphate

In principle, any known hydroxyethylthiazole kinase can be employed in the method according to the invention. In one aspect of the present invention, a hydroxyethylthiazole kinase of bacterial origin is used, such as a hydroxyethylthiazole kinase from a bacterium belonging to the genus Escherichia, Bacillus or Rhizobium, preferably of E. coli, Bacillus subtilis or of R. leguminosarum. Amino acid and nucleotide sequences for these enzymes are available. Examples for corresponding amino acid sequences are provided in SEQ ID NOs: 1 to 3. In a particularly preferred embodiment any protein showing an amino acid sequence as shown in any one of SEQ ID NOs: 1 to 3 or showing an amino acid sequence which is at least 80% homologous to any of SEQ ID NOs: 1 to 3 and having the activity of a hydroxyethylthiazole kinase can be employed in a method according to the present invention.

Moreover, in principle, any known thiamine kinase can be employed in the method according to the invention. In one aspect of the present invention, a thiamine kinase of bacterial origin is used, such as a thiamine kinase from a bacterium belonging to the genus Escherichia or Salmonella, preferably of E. coli or of Salmonella enterica. Amino acid and nucleotide sequences for these enzymes are available.

In one embodiment of this method, step A(ii) consists of a single enzymatic reaction in which crotyl phosphate is directly converted into butadiene. This option is in the following referred to as option A(ii1). In this conversion of crotyl phosphate into butadiene the phospho group is removed from crotyl phosphate with the simultaneous production of butadiene. An enzyme which can catalyze this reaction is referred to as a crotyl phosphate phosphate-lyase (butadiene forming). Examples of enzymes which can catalyze the dephosphorylation of crotyl phosphate into butadiene are enzymes which can be classified as belonging to the terpene synthase family. Preferably such an enzyme belongs to the family of plant terpene synthases. The terpene synthases constitute an enzyme family which comprises enzymes catalyzing the formation of numerous natural products always composed of carbon and hydrogen (terpenes) and sometimes also of oxygen or other elements (terpenoids). Terpenoids are structurally diverse and widely distributed molecules corresponding to well over 30000 defined natural compounds that have been identified from all kingdoms of life. In plants, the members of the terpene synthase family are responsible for the synthesis of the various terpene molecules from two isomeric 5-carbon precursor “building blocks”, isoprenyl diphosphate and prenyl diphosphate, leading to 5-carbon isoprene, 10-carbon monoterpene, 15-carbon sesquiterpene and 20-carbon diterpenes” (Chen et al.; The Plant Journal 66 (2011), 212-229).

The ability of terpene synthases to convert a prenyl diphosphate containing substrate to diverse products during different reaction cycles is one of the most unique traits of this enzyme class. The common key step for the biosynthesis of all terpenes is the reaction of terpene synthase on corresponding diphosphate esters. The general mechanism of this enzyme class induces the removal of the diphosphate group and the generation of an intermediate with carbocation as the first step. In the various terpene synthases, such intermediates further rearrange to generate the high number of terpene skeletons observed in nature. In particular, the resulting cationic intermediate undergoes a series of cyclizations, hydride shifts or other rearrangements until the reaction is terminated by proton loss or the addition of a nucleophile, in particular water for forming terpenoid alcohols (Degenhardt et al., Phytochemistry 70 (2009), 1621-1637).

The different terpene synthases share various structural features. These include a highly conserved C-terminal domain, which contains their catalytic site and an aspartate-rich DDXXD motif essential for the divalent metal ion (typically Mg2+ or Mn2+) assisted substrate binding in these enzymes (Green et al. Journal of biological chemistry, 284, 13, 8661-8669). In principle, any known enzyme which can be classified as belonging to the EC 4.2.3 enzyme superfamily can be employed for the conversion of crotyl phosphate into butadiene.

Even more preferably the method according to the invention makes use of an isoprene synthase (EC 4.2.3.27), a myrcene/ocimene synthase (EC 4.2.3.15), a farnesene synthase (EC 4.2.3.46 or EC 4.2.3.47) or a pinene synthase (EC 4.2.3.14). Also enzymes which are generally classified as monoterpene synthases can be used.

In a particularly preferred embodiment, the dephosphorylation of crotyl phosphate to butadiene is achieved by an isoprene synthase (EC 4.2.3.27). Isoprene synthase is an enzyme which catalyzes the following reaction:

Dimethylallyl diphosphateisoprene+diphosphate

This enzyme occurs in a number of organisms, in particular in plants and some bacteria. The occurrence of this enzyme has, e.g., been described for Arabidopsis thaliana, a number of Populus species like P. alba (UniProt accession numbers Q50L36, A9Q7C9, D8UY75 and D8UY76), P. nigra (UniProt accession number A0PFK2), P. canescence (UniProt accession number Q9AR86; see also Köksal et al., J. Mol. Biol. 402 (2010), P. tremuloides, P. trichocarpa, P. lobata, in Quercus petraea, Quercus robur, Salix discolour, Pueraria montana (UniProt accession number Q6EJ97), Mucuna pruriens, Vitis vinifera, Embryophyta and Bacillus subtilis. In principle, any known isoprene synthase can be employed in the method according to the invention. In a preferred embodiment, the isoprene synthase employed in a method according to the present invention is an isoprene synthase from a plant of the genus Populus, more preferably from Populus trichocarpa or Populus alba. In another preferred embodiment the isoprene synthase employed in a method according to the present invention is an isoprene synthase from Pueraria montana, preferably from Pueraria montana var. lobata (an example for such a sequence is provided in SEQ ID NO: 7), or from Vitis vinifera. Preferred isoprene synthases to be used in the context of the present invention are the isoprene synthase of Populus alba (Sasaki et al.; FEBS Letters 579 (2005), 2514-2518) or the isoprene synthases from Populus trichocarpa and Populus tremuloides which show very high sequence homology to the isoprene synthase from Populus alba. A particularly preferred isoprene synthase is the isoprene synthase from Pueraria montana var. lobata (kudzu) (Sharkey et al.; Plant Physiol. 137 (2005), 700-712). In a particularly preferred embodiment a protein showing an amino acid sequence as shown in SEQ ID NOs: 7 or showing an amino acid sequence which is at least 80% homologous to SEQ ID NOs: 7 and having the activity of an isoprene synthase can be employed in a method according to the present invention.

The activity of an isoprene synthase can be measured according to methods known in the art, e.g. as described in Silver and Fall (Plant Physiol (1991) 97, 1588-1591). In a typical assay, the enzyme is incubated with dimethylallyl diphosphate in the presence of the required co-factors, Mg²⁺ or Mn²⁺ and K⁺ in sealed vials. At appropriate time volatiles compound in the headspace are collected with a gas-tight syringe and analyzed for isoprene production by gas chromatography (GC). Crotyl monophosphate and crotyl diphosphate are structurally closely related to dimethylallyl diphosphate. In particular, the difference between crotyl diphosphate and dimethylallyl diphosphate is just a methyl group (see FIG. 8). The inventor considers that, therefore, an isoprene synthase can also use crotyl diphosphate or crotyl monophosphate as a substrate. In principle, any known isoprene synthase can be employed in the method according to the invention.

In another particularly preferred embodiment, the enzyme used for the conversion of crotyl phosphate into butadiene is a myrcene/ocimene synthases (EC 4.2.3.15). Myrcene/ocimene synthases (EC 4.2.3.15) are enzymes which naturally catalyze the following reaction:

Geranyl diphosphate(E)-beta-ocimene+diphosphate

or

Geranyl diphosphatemyrcene+diphosphate

These enzymes occur in a number of organisms, in particular in plants and animals, for example in Lotus japanicus, Phaseolus lunatus, Abies grandis, Arabidopsis thaliana (UniProt accession number Q9ZUH4), Actinidia chinensis, Perilla fructescens, Vitis vinifera, Ochtodes secundiramea and in Ips pini (UniProt accession number Q58GE8. In principle, any known myrcene/ocimene synthase can be employed in the method according to the invention. In a preferred embodiment, the myrcene/ocimene synthase employed in a method according to the present invention is a beta-ocimene synthase from Lotus japanicus (Arimura et al.; Plant Physiol. 135 (2004), 1976-1983; an example for such an enzyme is provided in SEQ ID NO: 9) or from Phaseolus lunatus (UniProt accession number B1P189; an example for such an enzyme is provided in SEQ ID NO: 10). In a particularly preferred embodiment the myrcene/ocimene synthase is an (E)-beta-ocimene synthase from Vitis vinifera (an example for such an enzyme is provided in SEQ ID NO: 12). In a particularly preferred embodiment any protein showing an amino acid sequence as shown in any one of SEQ ID NOs: 9, 10 or 12 or showing an amino acid sequence which is at least 80% homologous to any of SEQ ID NOs: 9, 10 or 12 and having the activity of a beta-ocimene synthase can be employed in a method according to the present invention.

The activity of an ocimene/myrcene synthase can be measured as described, for example, in Arimura et al. (Plant Physiology 135 (2004), 1976-1983. In a typical assay for determining the activity, the enzyme is placed in screwcapped glass test tube containing divalent metal ions, e.g. Mg²⁺ and/or Mn²⁺, and substrate, i.e. geranyl diphosphate. The aqueous layer is overlaid with pentane to trap volatile compounds. After incubation, the assay mixture is extracted with pentane a second time, both pentane fractions are pooled, concentrated and analyzed by gas chromatography to quantify ocimene/myrcene production.

Beta-farnesene synthases (EC 4.2.3.47) naturally catalyze the following reaction:

(2E,6E)-farnesyl diphosphate(E)-beta-farnesene+diphosphate

This enzyme occurs in a number of organisms, in particular in plants and in bacteria, for example in Artemisia annua (UniProt accession number Q4VM12), Citrus junos (UniProt accession number Q94JS8), Oryza sativa (UniProt accession number Q0J7R9), Pinus sylvestris (UniProt accession number D7PCH9), Zea diploperennis (UniProt accession number C7E5V9), Zea mays (UniProt accession numbers Q2NM15, C7E5V8 and C7E5V7), Zea perennis (UniProt accession number C7E5W0) and Streptococcus coelicolor (Zhao et al., J. Biol. Chem. 284 (2009), 36711-36719). In principle, any known beta-farnesene synthase can be employed in the method according to the invention. In a preferred embodiment, the beta-farnesene synthase employed in a method according to the present invention is a beta-farnesene synthase from Mentha piperita (Crock et al.; Proc. Natl. Acad. Sci. USA 94 (1997), 12833-12838).

Methods for the determination of farnesene synthase activity are known in the art and are described, for example, in Green et al. (Phytochemistry 68 (2007), 176-188). In a typical assay farnesene synthase is added to an assay buffer containing 50 mM BisTrisPropane (BTP) (pH 7.5), 10% (v/v) glycerol, 5 mM DTT. Tritiated farnesyl diphosphate and metal ions are added. Assays containing the protein are overlaid with 0.5 ml pentane and incubated for 1 h at 30° C. with gentle shaking. Following addition of 20 mM EDTA (final concentration) to stop enzymatic activity an aliquot of the pentane is removed for scintillation analysis. The olefin products are also analyzed by GC-MS.

Pinene synthase (EC 4.2.3.14) is an enzyme which naturally catalyzes the following reaction:

Geranyl diphosphatealpha-pinene+diphosphate

This enzyme occurs in a number of organisms, in particular in plants, for example in Abies grandis (UniProt accession number O244475), Artemisia annua, Chamaecyparis formosensis (UniProt accession number C3RSF5), Salvia officinalis and Picea sitchensis (UniProt accession number Q6XDB5).

For the enzyme from Abies grandis a particular reaction was also observed (Schwab et al., Arch. Biochem. Biophys. 392 (2001), 123-136), namely the following:

6,7-dihydrogeranyl diphosphate6,7-dihydromyrcene+diphosphate

In principle, any known pinene synthase can be employed in the method according to the invention. In a preferred embodiment, the pinene synthase employed in a method according to the present invention is a pinene synthase from Abies grandis (UniProt accession number O244475; Schwab et al., Arch. Biochem. Biophys. 392 (2001), 123-136).

Methods for the determination of pinene synthase activity are known in the art and are described, for example, in Schwab et al. (Archives of Biochemistry and Biophysics 392 (2001), 123-136). In a typical assay, the assay mixture for pinene synthase consists of 2 ml assay buffer (50 mM Tris/HCl, pH 7.5, 500 mM KCl, 1 mM MnCl2, 5 mM dithiothreitol, 0.05% NaHSO3, and 10% glycerol) containing 1 mg of the purified protein. The reaction is initiated in a Teflon-sealed screw-capped vial by the addition of 300 mM substrate. Following incubation at 25° C. for variable periods (0.5-24 h), the mixture is extracted with 1 ml of diethyl ether. The biphasic mixture is vigorously mixed and then centrifuged to separate the phases. The organic extract is dried (MgSO4) and subjected to GC-MS and MDGC analysis.

As indicated above, it is also possible to employ a monoterpene synthases in a method according to the invention. Particularly preferred are the monoterpene synthase from Melaleuca alternifolia described in Shelton et al. (Plant Physiol. Biochem. 42 (2004), 875-882; an example for such an enzyme is provided in SEQ ID NO: 11) or the monoterpene synthase from Eucalyptus globulus (UniProt accession number Q0PCI4; an example for such an enzyme is provided in SEQ ID NO: 8). In a particularly preferred embodiment any protein showing an amino acid sequence as shown in any one of SEQ ID NO: 11 or 8 or showing an amino acid sequence which is at least 80% homologous to any of SEQ ID NO: 11 or 8 and having the activity of a monoterpene synthase can be employed in a method according to the present invention.

The present inventors have shown that different types of terpene synthases, e.g. isoprene synthases, (E)-beta-ocimene and monoterpene synthase from different plant organisms are able to convert crotyl phosphate into butadiene (see Examples 12 and 13 and FIG. 11).

The reactions catalyzed by the various terpene synthases, in particular the terpene synthases mentioned above, show certain common features. For example, the reactions catalyzed by isoprene synthases, by myrcene/ocimene synthases, by farnesene synthases, by pinene synthase and by monoterpene synthases, respectively, are all believed to proceed through a common mechanism in which, in a first step a carbocation is created by elimination of the diphosphate (PP_i), which is then followed by direct deprotonation so as to form the corresponding diene. It could be shown by the present inventors that enzymes which belong to the family of terpene synthases are able to convert crotyl phosphate into butadiene.

In another embodiment of the method according to the invention step A(ii) consists of two enzymatic reactions comprising:

(a) the enzymatic conversion of crotyl phosphate into crotyl diphosphate; and
(b) the enzymatic conversion of crotyl diphosphate into butadiene.

This option is in the following referred to as option A(ii2) and the different steps are referred to as steps A(ii2a) and A(ii2b).

As regards step A(ii2a), the enzymatic conversion of crotyl phosphate into crotyl diphosphate can be achieved by the use of an enzyme which can catalyze the transfer of a phospho group onto a molecule, such as kinases. Preferably, ATP is the donor of the phospho group in such a reaction. The conversion can in particular, e.g., be achieved by the use of an isopentenyl phosphate kinase. This enzyme has so far not yet been classified and, therefore, no EC number is available. It is predicted to be a member of the amino acid kinase superfamily, in particular the aspartokinase superfamily. The enzyme isopentenyl phosphate kinase catalyzes the following reaction:

Isopentenyl phosphate+ATPisopentenyl diphosphate+ADP

This enzyme participates in an alternative branch of the mevalonate pathway which has been discovered in the archaeon Methanocaldococcus jannaschii. It is a small molecule kinase. The primary amino acid sequence and the crystal structure of the isopentenyl phosphate kinase of Methanocaldococcus jannaschii has already been disclosed as well as mutants which are able to use oligoprenyl monophosphates as substrate (Dellas and Noel, ACS Chem. Biol. 5 (2010), 589-601). The active site has been characterized and the amino acid residues crucial for binding and catalysis of the reaction have been identified. Because of the high structural similarity of isopentenyl phosphate and crotyl phosphate and the fact that mutants of the isopentenyl phosphate kinase of Methanocaldococcus jannaschii have already been shown to be able to use other oligoprenyl monophosphates as substrates, it can be expected that this enzyme or mutants thereof will also be able to convert crotyl phosphate into crotyl diphosphate. The sequence of the isopentenyl phosphate kinase from Methanocaldococcus jannaschii is shown in SEQ ID NO: 6.

Genes encoding an isopentenyl phosphate kinase are also known from Methanothermobacter thermautotrophicus (MTH) and from Thermoplasma acidophilum (THA) (Chen and Poulter, Biochemistry 49 (2010), 207-217). For both these enzymes crystal structures have been determined (Mabanglo et al., ACS Chem. Biol. 5 (2010), 517-527). The sequence of the isopentenyl phosphate kinase from Methanothermobacter thermautotrophicus is shown in SEQ ID NO: 5. The sequence of the isopentenyl phosphate kinase from Thermoplasma acidophilum is shown in SEQ ID NO: 4. In a particularly preferred embodiment any protein showing an amino acid sequence as shown in any one of SEQ ID NOs: 4 to 6 or showing an amino acid sequence which is at least 80% homologous to any of SEQ ID NOs: 4 to 6 and having the activity of an isopentenyl phosphate kinase can be employed in a method according to the present invention.

As regards step A(ii2b), the enzymatic conversion of crotyl diphosphate into butadiene involves the removal of a diphosphate group from crotyl diphosphate with the simultaneous production of butadiene. An enzyme which can catalyze this reaction is referred to as a crotyl diphosphate diphosphate-lyase (butadiene forming). Examples of enzymes which can catalyze the dephosphorylation of crotyl diphosphate into butadiene are enzymes which can be classified as belonging to the terpene synthase family. Preferably such an enzyme belongs to the family of plant terpene synthases. These enzymes have already been disclosed in detail hereinabove in connection with the conversion of crotyl phosphate into butadiene and the same applies here.

Preferably the terpene synthase is an isoprene synthase (EC 4.2.3.27), a myrcene/ocimene synthase (EC 4.2.3.15), a farnesene synthase (EC 4.2.3.46 or EC 4.2.3.47) or a pinene synthase (EC 4.2.3.14). Also enzymes which are generally classified as monoterpene synthases can be used. Particularly preferred the terpene synthase is an isoprene synthase, an (E)-beta ocimene synthase or a monoterpene synthase.

In a particularly preferred embodiment the dephosphorylation of crotyl diphosphate into butadiene is achieved by the use of an isoprene synthase (EC 4.2.3.27). As regards the isoprene synthase to be employed in the method, the same applies as has been described herein above. In a particularly preferred embodiment the isoprene synthase employed is an isoprene synthase from P. montana var. lobata. As explained above, crotyl diphosphate is structurally closely related to dimethylallyl diphosphate. Therefore, it is considered that an isoprene synthase can also use crotyl diphosphate as a substrate and can convert it into butadiene.

In another particularly preferred embodiment, the dephosphorylation of crotyl diphosphate into butadiene is achieved by the use of a myrcene/ocimene synthase (EC 4.2.3.15). As regards the myrcene/ocimene synthase to be employed in the method, the same applies as has been described herein above. In a particularly preferred embodiment the myrcene/ocimene synthase employed is an (E)-beta ocimene synthase, most preferably an (E)-beta ocimene synthase from Vitis vinifera or from L. japonicus or from P. lunatus.

In another particularly preferred embodiment, the dephosphorylation of crotyl diphosphate into butadiene is achieved by the use of a monoterpene synthase. As regards the monoterpene synthase to be employed in the method, the same applies as has been described herein above. In a particularly preferred embodiment the monoterpene synthase employed is a monoterpene synthase from Eucalyptus globulus.

The present inventors have shown that different types of terpene synthases, e.g. isoprene synthase, (E)-beta-ocimene and monoterpene synthase from different plant organisms are able to convert crotyl diphosphate into butadiene (see Examples 14 and 15 and FIG. 13).

In another aspect (B), the method according to the invention comprises the two enzymatic steps of

(I) enzymatically converting crotyl alcohol into crotyl diphosphate; and
(II) enzymatically converting crotyl diphosphate into butadiene.

This alternative is in the following referred to as Alternative B and the different steps are referred to as B(I) and B(II).

In this embodiment the enzymatic conversion of crotyl alcohol into crotyl diphosphate according to step B(I) consists of a single enzymatic reaction in which crotyl alcohol is directly converted into crotyl diphosphate.

The direct enzymatic conversion of crotyl alcohol into crotyl diphosphate in one step can, e.g., be achieved by the use of an enzyme which is able to catalyze the transfer of a diphosphate group, such as a diphosphotransferase, for example enzymes which are classified as EC 2.7.6 (diphosphotransferases). Examples are 2-amino-4-hydroxy-6-hydroxymethyldihydropteridine diphosphokinase (EC 2.7.6.3) and thiamine diphosphokinase (EC 2.7.6.2). Preferably, ATP is the donor of the diphosphate group in such a reaction.

Thus, in one embodiment the direct enzymatic conversion of crotyl alcohol into crotyl diphosphate in one step can be achieved by the use of a 2-amino-4-hydroxy-6-hydroxymethyldihydropteridine diphosphokinase (EC 2.7.6.3). This enzyme catalyzes the following reaction:

2-amino-4-hydroxy-6-hydroxymethyl-7,8-dihydropteridine+ATP2-amino-7,8-dihydro-4-hydroxy-6-(diphosphooxymethyl)pteridine+AMP

The occurrence of this enzyme has been described for several organisms, e.g. for E. coli, Plasmodium falciparum, Plasmodium chabaudi, Streptococcus pneumoniae, Toxoplasma gondii, Yersinia pestis, Pneumocystis carinii, Haemophilus influenzae, S. cerevisiae, Arabidopsis thaliana and Pisum sativum.

In principle, any known 2-amino-4-hydroxy-6-hydroxymethyldihydropteridine diphosphokinase can be employed in the method according to the invention.

In another embodiment the direct enzymatic conversion of crotyl alcohol into crotyl diphosphate in one step can be achieved by the use of a thiamine diphosphokinase (EC 2.7.6.2). This enzyme catalyzes the following reaction:

ATP+thiamineAMP+thiamine diphosphate

The occurrence of this enzyme has been described for several organisms, e.g. for Salmonella enterica, Plasmodium falciparum, Saccharomyces cerevisiae, Schizosaccharomyces pombe, Candida albicans, Arabidopsis thaliana, Caenorhabditis elegans, Rattus norvegicus, Mus musculus and Homo sapiens. In principle, any known thiamine diphosphokinase can be employed in the method according to the invention.

In step B(II) the obtained crotyl diphosphate is then further converted enzymatically into butadiene. This enzymatic conversion of crotyl diphosphate into butadiene involves the removal of a diphosphate group and can, e.g., be achieved by the use of terpene synthase as described herein above. As regards the preferred embodiments, the same applies as set forth herein above.

In a particularly, preferred embodiment an isoprene synthase (EC 4.2.3.27) is employed for the conversion of crotyl diphosphate into butadiene.

The crotyl alcohol which is used as a substrate for the enzymatic production of butadiene according to the invention can either be supplied externally or it can itself be provided by the reduction of crotonaldehyde (but-2-enal). This reduction can, e.g., be achieved by chemical reactions as known to the person skilled in the art. However, according to the present invention it is preferable that the provision of crotyl alcohol is achieved by the enzymatic conversion of crotonyl-Coenzyme A (in the following crotonyl-CoA; see FIG. 9) or of crotonaldehyde into crotyl alcohol. Thus, in another embodiment the method according to the invention further comprises the step of providing crotyl alcohol by the enzymatic conversion of crotonaldehyde into crotyl alcohol as described herein below. Crotonaldehyde (CH₃CH═CHCHO; (2E)-but-2-enal) occurs naturally, e.g. in soybean oils, and can be synthesized chemically by the aldol condensation of acetaldehyde. Alternatively, the method according to the invention further comprises the step of providing crotyl alcohol by the enzymatic conversion of crotonyl-CoA into crotyl alcohol as described below. Crotonyl-coenzyme A is a thioester between crotonic acid and Coenzyme A. It is an intermediate in the fermentation of butyric acid, and in the metabolism of lysine and tryptophan. During degradation of these amino acids, α-ketoadipate is produced which is converted into glutaryl-CoA by oxidative decarboxylation. Glutaryl-CoA is then converted by glutaryl-CoA dehydrogenase into crotonyl-CoA, which can be converted in two further steps into two molecules of acetyl-CoA. Crotonyl-CoA is also a metabolite in the fermentation of glucose by some obligatory anaerobe bacteria in which butyric acid is produced, such as Clostridium acetobutylicum. Moreover, crotonyl-CoA had been isolated in some microorganisms which assimilate acetate via the so-called ethyl-malonyl-CoA pathway. It also occurs as an intermediate in some metabolic pathways leading to the assimilation of carbon dioxide, e.g. in the 3-hydroxyproprionate/4-hydroxybutyrate cycle or the dicarboxylate/4-hydroxybutyrate cycle.

The present inventor also developed a method for enzymatically producing crotyl alcohol enzymatically starting from crotonaldehyde or from crotonyl-CoA.

Thus, in a second aspect, the present invention relates to a method for producing crotyl alcohol. Such a method comprises the enzymatic conversion of crotonyl-CoA into crotonaldehyde and the subsequent enzymatic conversion of crotonaldehyde into crotyl alcohol. The first reaction may occur according to the following schemes:

Crotonyl-CoA+NADH+H⁺crotonaldehyde+CoA+NAD⁺

or

Crotonyl-CoA+NADPH+H⁺crotonaldehyde+CoA+NADP⁺

This reaction is a reduction and can be catalyzed by various enzymes. In one aspect, it is possible to use for the above indicated conversion of crotonyl-CoA to crotonaldehyde a hydroxymethylglutaryl-CoA reductase (EC 1.1.1.34). This enzyme normally catalyzes the following reaction

(S)-3-hydroxy-methylglutaryl-CoA+2NADPH+H⁺(R)-mevalonate+CoA+2NADP⁺

Enzymes belonging to this class and catalyzing the above shown conversion occur in organisms of all kingdoms, i.e. plants, animals, fungi, bacteria etc. and have extensively been described in the literature. Nucleotide and/or amino acid sequences for such enzymes have been determined for numerous organisms, in particular bacterial organisms. In principle, any hydroxymethylglutaryl-CoA reductase (EC 1.1.1.34) can be used in the context of the present invention.

Alternatively or in addition, the above described conversion of crotonyl-CoA into crotonaldehyde can also be achieved by using an enzyme referred to as acetaldehyde dehydrogenase (EC 1.2.1.10). This enzyme normally catalyzes the following reaction

Acetyl-CoA+NADH+H⁺acetaldehyde+CoA+NAD⁺

Enzymes belonging to this class and catalyzing the above shown conversion occur in several types of bacteria, like e. coli, Acinetobacter sp., Leuconostoc mesenteroides, Pseudomonas sp, Clostridium beijerinckii, Clostridium kluyveri, Giardia intestinalis, Propionibacterium freudenreichii and Thermoanaerobacter ethanolicus In principle, any acetaldehyde dehydrogenase (EC 1.2.1.10) can be used in the context of the present invention.

Alternatively or in addition, the above described conversion of crotonyl-CoA into crotonaldehyde can also be achieved by using an enzyme referred to as aldehyde-alcohol dehydrogenase, such as the aldehyde-alcohol dehydrogenase as encoded by an adhE gene. Such an enzyme is bifunctional in that it shows at least the enzymatic activities of an alcohol dehydrogenase and an aldehyde dehydrogenase, such as an acetaldehyde dehydrogenase. An example for such an enzyme is the aldehyde-alcohol dehydrogenase of E. coli (adhE; UniProtKB/Swiss-Prot Accession number P0A9Q7; Jul. 27, 2011; Version 58). Corresponding enzymes are also known from other organisms, such as, e.g. Leuconostoc mesenteroides (Koo et al., Biotechnology Letters 27, 505-510), Polytomella sp. and Chlamydomonas reinhardtii (Atteia et al., Plant Mal. Biol. 53 (2003), 175-188). Genes encoding such enzymes have been found in the genomes of several Gram-positive bacteria belonging to the categories bacilli and clostridia, in several gamma-proteobacteria, in actinobacteria, in cyanobacteria and some amitochondriate protists (see Atteia et al., loc. cit.).

Alternatively or in addition, the above described conversion of crotonyl-CoA into crotonaldehyde can also be achieved by using enzymes referred to as acyl-CoA reductases. Examples for such enzymes are cinnamoyl-CoA reductase (EC 1.2.1.44), long-chain-fatty-acyl-CoA reductase (EC 1.2.1.50) and malonyl-CoA reductase (malonate semialdehyde-forming; EC 1.2.1.75).

According to the present invention the produced crotonaldehyde is further converted into crotyl alcohol. The enzymatic conversion of crotonaldehyde into crotyl alcohol is a reduction/hydrogenation and may occur according to the following schemes:

Crotonaldehyde+NADH+H⁺crotyl alcohol+NAD⁺

or

Crotonaldehyde+NADPH+H⁺crotyl alcohol+NADP⁺

This reaction can be catalyzed by various enzymes. In one aspect, it is possible to use for the above indicated conversion of crotonaldehyde to crotyl alcohol an enzyme which is known to be able to catalyze this reaction. One example is the aldo-keto reductase (AKR) encoded by the sakR1 gene. This enzyme had been identified in Synechococcus sp. PCC 7002 and has been described in Dongyi et al. (Microbiol. 152 (2006), 2013-2021). It uses NADPH/NADP⁺ as a cofactor. Another example is the aldo-keto reductase (AKR) encoded by the At2g37770 gene, which had been identified in Arabidopsis (Yamauchii et al. (J. Biol. Chem. 286 (2011) 6999-7009). It uses NADPH/NADP⁺ as a cofactor. A further example is the 321-MB dehydrogenase from the soil bacterium Pseudomonas putida MB-1 (Malone et al., Appl. Environm. Microbiol. 65 (1999), 2622-2630) which uses NADH/NAD⁺ as a cofactor.

In another embodiment it is also possible to use for the above indicated conversion of crotonaldehyde to crotyl alcohol a hydroxymethylglutaryl-CoA reductase (EC 1.1.1.34). This enzyme has already been described above and that what had been said above holds also true for this reaction.

Alternatively or in addition, the above described conversion of crotonaldehyde into crotyl alcohol can also be achieved by using an alcohol dehydrogenase (EC 1.1.1.1). Such an enzyme normally catalyzes the following reaction

Primary alcohol+NAD⁺aldehyde+NADH+H⁺

Enzymes belonging to this class and catalyzing the above shown conversion occur in organisms of all kingdoms, i.e. plants, animals, fungi, bacteria etc. and have extensively been described in the literature. Nucleotide and/or amino acid sequences for such enzymes have been determined for numerous organisms, in particular bacterial organisms. In principle, any alcohol dehydrogenase (EC 1.1.1.1) can be used in the context of the present invention.

Moreover, the conversion of crotonaldehyde to crotyl alcohol can also be achieved by the use of an enzyme referred to as an aldehyde reductase. Examples for such enzymes are alcohol dehydrogenase (NADP⁺; EC 1.1.1.2), allyl-alcohol dehydrogenase (EC 1.1.1.54), retinol dehydrogenase (EC 1.1.1.105), sulcatone dehydrogenase (EC 1.1.1.260) and 3-methylbutanal reductase (EC 1.1.1.265)

The enzymatic conversion of crotonyl-CoA into crotyl alcohol may also occur according to the following schemes:

Crotonyl-CoA+2NADH+2H⁺crotyl alcohol+CoA+2NAD⁺

or

Crotonyl-CoA+2NADPH+2H⁺crotyl alcohol+CoA+2NADP⁺

Similar to the above described conversions, this reaction goes via crotonaldehyde as an intermediate. However, in this embodiment of the invention, the conversion of crotonyl-CoA into crotyl alcohol is catalyzed by one enzyme which catalyses both reduction/hydrogenation steps. An enzyme which may be employed in this conversion is an aldehyde-alcohol dehydrogenase, such as the aldehyde-alcohol dehydrogenase as encoded by an adhE gene which had already been described above.

Another enzyme which may be used in this conversion is a hydroxymethylglutaryl-CoA reductase (EC 1.1.1.34) which has already been described above. In a further preferred embodiment the conversion of crotonyl-CoA into crotyl alcohol is achieved by the use of a short-chain dehydrogenase/fatty acyl-CoA reductase.

The term “short-chain dehydrogenase/fatty acyl-CoA reductase” or “short-chain dehydrogenases/reductases (SDR)” in the context of the present invention refers to enzymes which are characterized by the following features:

• 1. They catalyze a two-step reaction in which fatty acy-CoA is reduced to fatty alcohol.
• 2. They show a substrate specificity for acyl-CoA containing an aliphatic chain from 8 to 20 carbon atoms.

Preferably such enzymes are furthermore characterized by the feature that they show a specific motif in their primary structure, i.e. amino acid sequence, namely they show two specific glycine motifs for NADP(H) binding.

The short-chain dehydrogenase/fatty acyl-CoA reductase or short-chain dehydrogenases/reductases (SDR) enzymes constitute a family of enzymes, most of which are known to be NAD- or NADP-dependent oxidoreductase (Jornvall H. et al., Biochemistry 34 (1995), 6003-6013). Recently, a novel bacterial NADP-dependent reductase from Marinobacter aquaeolei VT8 was characterized (Willis et al., Biochemistry 50 (2011), 10550-10558). This enzyme catalyzes the four-electron reduction of fatty acyl-CoA substrates to the corresponding fatty alcohols. The enzymatic conversion of fatty acyl-CoA into fatty alcohol occurs through an aldehyde intermediate according to the following scheme:

The enzyme displays activity on fatty acyl-CoA substrates ranging from 8 to 20 carbons in length (both saturated and unsaturated) as well as on fatty aldehyde substrates. Characteristically, proteins of this family possess two NAD(P)(H)-binding motifs, which have the conserved sequence GXGX(1-2×)G (Willis et al., Biochemistry 50 (2011), 10550-10558; Jornvall H. et al., Biochemistry 34 (1995), 6003-6013). The first pattern, GTGFIG, is identified near the N-terminus and the second signature sequence, GXXXGXG, is located between residues 384-390.

In principle any “short-chain dehydrogenase/fatty acyl-CoA reductase” or “short-chain dehydrogenases/reductases (SDR)” can be applied in the method according to the invention.

Preferably, the short-chain dehydrogenase/fatty acyl-CoA reductase is a short-chain dehydrogenase/fatty acyl-CoA reductase from a marine bacterium, preferably from the genus Marinobacter or Hahella, even more preferably from the species Marinobacter aquaeolei, more preferably Marinobacter aquaeolei VT8, Marinobacter manganoxydans, Marinobacter algicola, Marinobacter sp. ELB17 or Hahelly chejuensis. Examples of such enzymes are the short-chain dehydrogenase/fatty acyl-CoA reductase from Marinobacter aquaeolei VT8 (Uniprot accession number A1U3L3; Willis et al., Biochemistry 50 (2011), 10550-10558), the short-chain dehydrogenase from Marinobacter manganoxydans (Uniprot accession number G6YQS9), the short-chain dehydrogenase from Marinobacter algicola (Uniprot accession number A6EUH6), the short-chain dehydrogenase from Marinobacter sp. ELB17 (Uniprot accession number A3JCC5) and the short-chain dehydrogenase from Hahella chejuensis (Uniprot accession number Q2SCE0).

The sequence of the short-chain dehydrogenase/fatty acyl-CoA reductase from Marinobacter aquaeolei VT8 is shown in SEQ ID NO: 13. The sequence of the short-chain dehydrogenase/fatty acyl-CoA reductase from Marinobacter manganoxydans is shown in SEQ ID NO: 14. The sequence of the short-chain dehydrogenase/fatty acyl-CoA reductase from Marinobacter sp. ELB17 is shown in SEQ ID NO: 15. The sequence of the short-chain dehydrogenase/fatty acyl-CoA reductase from Marinobacter algicola is shown in SEQ ID NO: 16. The sequence of the short-chain dehydrogenase/fatty acyl-CoA reductase from Hahella chejuensis is shown in SEQ ID NO: 17. In a particularly preferred embodiment any protein showing an amino acid sequence as shown in any one of SEQ ID NOs: 13 to 17 or showing an amino acid sequence which is at least 80% homologous to any of SEQ ID NOs: 13 to 17 and having the activity of a short-chain dehydrogenase/fatty acyl-CoA reductase can be employed in a method according to the present invention.

The methods according to the first and second aspect of the present invention as described above may also be combined, i.e. it is possible that a method according to the first aspect of the invention for the production of butadiene from crotyl alcohol further comprises the steps of a method according to the second aspect of the invention for the provision of crotyl alcohol by enzymatic reactions as described above.

In another embodiment the methods according to the first and/or second aspect of the invention may also include the further step of enzymatically providing crotonyl-CoA. This may be achieved by the enzymatic conversion of 3-hydroxybutyryl-Coenzyme A into crotonyl-Coenzyme A. This reaction may occur according to the following scheme:

3-hydroxybutyryl-Coenzyme Acrotonyl-Coenzyme A+H₂O

This reaction corresponds to a Michael elimination and can, for example, be catalyzed by an enzyme called 3-hydroxybutyryl-CoA dehydratase which is classified as EC 4.2.1.55. This enzyme belongs to the family of lyases, specifically the hydro-lyases, which cleave carbon-oxygen bonds. The systematic name of this enzyme class is (3R)-3-hydroxybutanoyl-CoA hydro-lyase (crotonoyl-CoA-forming). Other names in common use include D-3-hydroxybutyryl coenzyme A dehydratase, D-3-hydroxybutyryl-CoA dehydratase, enoyl coenzyme A hydrase (D), and (3R)-3-hydroxybutanoyl-CoA hydro-lyase. This enzyme participates in butanoate metabolism. Enzymes belonging to this class and catalyzing the above shown conversion of 3-hydroxybutyryl-Coenzyme A into crotonyl-Coenzyme A have been described to occur, e.g. in rat (Rattus norvegicus) and in Rhodospirillum rubrum. Nucleotide and/or amino acid sequences for such enzymes have been determined, e.g. for Aeropyrum pernix. In principle, any 3-hydroxybutyryl-CoA dehydratase (EC 4.2.1.55) can be used in the context of the present invention.

Alternatively or in addition, the above described conversion of 3-hydroxybutyryl-Coenzyme A into crotonyl-Coenzyme A can also be achieved by using an enzyme referred to as enoyl-CoA hydratase (EC 4.2.1.17). Enoyl-CoA hydratase is an enzyme that normally hydrates the double bond between the second and third carbons on acyl-CoA. However, it can also be employed to catalyze the reaction in the reverse direction. This enzyme, also known as crotonase, is naturally involved in metabolizing fatty acids to produce both acetyl-CoA and energy. Enzymes belonging to this class have been described to occur, e.g. in rat (Rattus norvegicus), humans (Homo sapiens), mouse (Mus musculus), wild boar (Sus scrofa), Bos taurus, E. coli, Clostridium acetobutylicum and Clostridium aminobutyricum. Nucleotide and/or amino acid sequences for such enzymes have been determined, e.g. for rat, humans and Bacillus subtilits. In principle, any enoyl-CoA hydratase (EC 4.2.1.17) can be used in the context of the present invention.

In another embodiment it is also possible to use for the above described conversion of 3-hydroxybutyryl-Coenzyme A into crotonyl-Coenzyme A an enoyl-CoA hydratase 2 (EC 4.2.1.119) or a crotonyl-[acyl-carrier-protein] hydratase (EC 4.2.1.58).

In another embodiment the methods according to the first and/or second aspect of the invention may also include the further step of enzymatically providing 3-hydroxybutyryl-Coenzyme A. This can be achieved by the enzymatic conversion of acetoacetyl-CoA into 3-hydroxybutyryl-Coenzyme A. This reaction may occur according to the following scheme:

acetoacetyl-CoA+NADH+H⁺3-hydroxybutyryl-Coenzyme A+NAD⁺

or

acetoacetyl-CoA+NADPH+H⁺3-hydroxybutyryl-Coenzyme A+NADP⁺

This reaction is a reduction and can, e.g., be catalyzed by an enzyme called acetoacetyl-CoA reductase which is classified as EC 1.1.1.36. Enzymes belonging to this class and catalyzing the above shown conversion of acetoactyl-CoA into 3-hydroxybutyryl-Coenzyme A occur in organisms of all kingdoms, i.e. plants, animals, fungi, bacteria etc. and have extensively been described in the literature. Nucleotide and/or amino acid sequences for such enzymes have been determined for numerous organisms, in particular bacterial organisms. In principle, any acetoacetyl-CoA reductase (EC 1.1.1.36) can be used in the context of the present invention. In one embodiment the enzyme employed in the method according to the invention originates from E. coli.

In yet a further embodiment the methods according to the first and/or second aspect of the invention may also include the further step of enzymatically providing acetoacetyl-CoA. This can be achieved by the enzymatic conversion of two molecules acetyl-CoA into one molecule of acetoacetyl-CoA. Acetyl-CoA is a metabolic intermediate which occurs in all living organisms and plays a central role in metabolism. Thus, according to the present invention, acetyl-CoA can, for example, be converted into acetoacetyl-CoA by the following reaction:

2 acetyl-CoAacetoacetyl-CoA CoA

This reaction is catalyzed by enzymes called acetyl-CoA C-acetyltransferases which are classified as EC 2.3.1.9. Enzymes belonging to this class and catalyzing the above shown conversion of two molecules of acetyl-CoA into acetoacetyl-CoA and CoA occur in organisms of all kingdoms, i.e. plants, animals, fungi, bacteria etc. and have extensively been described in the literature. Nucleotide and/or amino acid sequences for such enzymes have been determined for a variety of organisms, like Homo sapiens, Arabidopsis thaliana, E. coli, Bacillus subtilis and Candida, to name just some examples. In principle, any acetyl-CoA C-acetyltransferase (EC 2.3.1.9) can be used in the context of the present invention.

Alternatively, the provision of acetoacetyl-CoA may also be achieved by the enzymatic conversion of acetyl-CoA and malonyl-CoA into acetoacetyl-CoA. This reaction is catalyzed by an enzyme called acetoacetyl-CoA synthase. The gene encoding this enzyme was identified in the mevalonate pathway gene cluster for terpenoid production in a soil-isolated Gram-positive Streptomyces sp. Strain CL190 (Okamura et al., PNAS USA 107 (2010) 11265-11270, 2010). Moreover a biosynthetic pathway using this enzyme for acetoacetyl-CoA production was recently developed in E. coli (Matsumoto K et al., Biosci. Biotechnol. Biochem, 75 (2), 364-366, 2011, enclosed)

The methods according to the present invention may be carried out in vitro or in vivo. An in vitro reaction is understood to be a reaction in which no cells are employed, i.e. an acellular reaction. Thus, in vitro preferably means in a cell-free system. The term “in vitro” in one embodiment means in the presence of isolated enzymes (or enzyme systems optionally comprising possibly required cofactors). In one embodiment, the enzymes employed in the method are used in purified form. For carrying out the process in vitro the substrates for the reaction and the enzymes are incubated under conditions (buffer, temperature, cosubstrates, cofactors etc.) allowing the enzymes to be active and the enzymatic conversion to occur. The reaction is allowed to proceed for a time sufficient to produce butadiene. The production of butadiene can be measured by methods known in the art, such as gas chromatography possibly linked to mass spectrometry detection.

The enzymes may be in any suitable form allowing the enzymatic reaction to take place. They may be purified or partially purified or in the form of crude cellular extracts or partially purified extracts. It is also possible that the enzymes are immobilized on a suitable carrier.

In one embodiment of the method according to the invention the substrate which is used in such an in vitro method is crotyl alcohol which is converted by the use of the above-mentioned enzymes to butadiene. In another embodiment, the substrate used in such an in vitro method is crotonaldehyde which is first converted into crotyl alcohol as described above which is then in turn converted into butadiene as described above.

The in vitro method according to the invention may be carried out in a one-pot-reaction, i.e. the substrate is combined in one reaction mixture with the above described enzymes necessary for the conversion into butadiene and the reaction is allowed to proceed for a time sufficient to produce butadiene. Alternatively, the method may also be carried out by effecting one or more enzymatic steps in a consecutive manner, i.e. by first mixing the substrate with one or more enzymes and allowing the reaction to proceed to an intermediate and then adding one or more further enzymes to convert the intermediate further either into an intermediate or into butadiene.

The in vitro method according to the invention furthermore may comprise the step of collecting gaseous products, in particular butadiene, degassing out of the reaction, i.e. recovering the products which degas, e.g., out of the culture. Thus, in one embodiment, the method is carried out in the presence of a system for collecting butadiene under gaseous form during the reaction.

As a matter of fact, butadiene adopts the gaseous state at room temperature and atmospheric pressure. The method according to the invention therefore does not require extraction of the product from the reaction mixture, a step which is always very costly when performed at industrial scale. The evacuation and storage of butadiene and its possible subsequent physical separation from other gaseous substances as well as its chemical conversion can be performed according to any method known to one of skill in the art. For example, butadiene can be separated from CO₂ by the condensation of CO₂ at low temperatures. CO₂ can also be removed by polar solvents, e.g. ethanolamine. Moreover, it can be isolated by adsorption on a hydrophobic membrane.

In another embodiment the method according to the invention is carried out in culture, in the presence of an organism, preferably a microorganism, producing at least the enzymes described above which are necessary to produce butadiene according to a method of the invention according to the first aspect by using one of the alternative routes A or B described above and starting either from crotyl alcohol or from crotonaldehyde. Thus, in such an embodiment of the invention, an organism, preferably a microorganism, that produces the enzymes specified in the description of alternatives A or B, above, is used. It is possible to use a (micro)organism which naturally produces one or more of the required enzymes and to genetically modify such a (micro)organism so that it expresses also those enzymes which it does not naturally express. Preferably a (micro)organism is used which has been genetically modified as described hereinabove in connection with the second aspect of the invention so as to be able to produce crotyl alcohol.

In alternative A1 it is for example possible to use Bacillus subtilis which possesses a gene encoding the enzyme hydroxyethylthiazole kinase and a gene encoding, a terpene synthase, e.g. an isoprene synthase. Such a bacterium may be further genetically modified as described herein above so as to be able to produce crotyl alcohol.

In alternative B it is, e.g., possible to use E. coli or S. cerevisiae, which both possess a gene encoding 2-amino-4-hydroxy-6-hydroxymethyldihydropteridine diphosphokinase, and to introduce into such a microorganism a gene, for example from Bacillus subtilis encoding a terpene synthase, e.g. an isoprene synthase. Similarly, it is possible to use in alternative B as a microorganism B. subtilis and to genetically modify it with a gene encoding a 2-amino-4-hydroxy-6-hydroxymethyldihydropteridine diphosphokinase, e.g. from E. coli or from S. cerevisiae. Again, such microorganisms may be further genetically modified as described herein above so as to be able to produce crotyl alcohol.

If a (micro)organism is used which naturally expresses one of the required enzyme activities, it is possible to modify such a (micro)organism so that this activity is overexpressed in the (mircro)organism. This can, e.g., be achieved by effecting mutations in the promoter region of the corresponding gene so as to lead to a promoter which ensures a higher expression of the gene. Alternatively, it is also possible to mutate the gene as such so as to lead to an enzyme showing a higher activity.

By using (micro)organisms which express the enzymes which are necessary according to alternative A or B as described above, it is possible to carry out the method according to the invention directly in the culture medium, without the need to separate or purify the enzymes.

In one embodiment, a (micro)organism is used having the natural or artificial property of endogenously producing crotyl alcohol, and also expressing or overexpressing the enzymes as described in connection with alternatives A and B, above, so as to produce butadiene directly from a carbon source present in solution. In another embodiment, the (micro)organism which is used has the natural or artificial property of endogenously producing crotonaldehyde and to convert it into crotyl alcohol which can then be further converted into butadiene.

In one embodiment the organism employed in the method according to the invention is an organism, preferably a microorganism, which has been genetically modified to contain one or more foreign nucleic acid molecules encoding one or more of the enzymes as described above in connection with alternatives A or B. The term “foreign” in this context means that the nucleic acid molecule does not naturally occur in said organism/microorganism. This means that it does not occur in the same structure or at the same location in the organism/microorganism. In one preferred embodiment, the foreign nucleic acid molecule is a recombinant molecule comprising a promoter and a coding sequence encoding the respective enzyme in which the promoter driving expression of the coding sequence is heterologous with respect to the coding sequence. Heterologous in this context means that the promoter is not the promoter naturally driving the expression of said coding sequence but is a promoter naturally driving expression of a different coding sequence, i.e., it is derived from another gene, or is a synthetic promoter or a chimeric promoter. Preferably, the promoter is a promoter heterologous to the organism/microorganism, i.e. a promoter which does naturally not occur in the respective organism/microorganism. Even more preferably, the promoter is an inducible promoter. Promoters for driving expression in different types of organisms, in particular in microorganisms, are well known to the person skilled in the art.

In a further embodiment the nucleic acid molecule is foreign to the organism/microorganism in that the encoded enzyme is not endogenous to the organism/microorganism, i.e. is naturally not expressed by the organism/microorganism when it is not genetically modified. In other words, the encoded enzyme is heterologous with respect to the organism/microorganism. The foreign nucleic acid molecule may be present in the organism/microorganism in extrachromosomal form, e.g. as a plasmid, or stably integrated in the chromosome. A stable integration is preferred. Thus, the genetic modification can consist, e.g. in integrating the corresponding gene(s) encoding the enzyme(s) into the chromosome, or in expressing the enzyme(s) from a plasmid containing a promoter upstream of the enzyme-coding sequence, the promoter and coding sequence preferably originating from different organisms, or any other method known to one of skill in the art.

In a preferred embodiment the (micro)organism of the present invention is also genetically modified so as to be able to produce crotyl alcohol as described herein above.

The organisms used in the invention can be prokaryotes or eukaryotes, preferably, they are microorganisms such as bacteria, yeasts, fungi or molds, or plant cells or animal cells. In a particular embodiment, the microorganisms are bacteria, preferably of the genus Escherichia or Bacillus and even more preferably of the species Escherichia coli or Bacillus subtilis.

In another embodiment, the microorganisms are recombinant bacteria of the genus Escherichia or Bacillus, preferably of the species Escherichia coli or Bacillus subtilis, having been modified so as to endogenously produce crotyl alcohol and to convert it into butadiene.

It is also possible to employ an extremophilic bacterium such as Thermus thermophilus, or anaerobic bacteria from the family Clostridiae.

In one embodiment the microorganism is a fungus, more preferably a fungus of the genus Saccharomyces, Schizosaccharomyces, Aspergillus, Trichoderma, Pichia or Kluyveromyces and even more preferably of the species Saccharomyces cerevisiae, Schizosaccharomyces pombe, Aspergillus niger, Trichoderma reesei, Pichia pastoris or of the species Kluyveromyces lactis. In a particularly preferred embodiment the microorganism is a recombinant yeast capable of producing crotyl alcohol and converting it into butadiene due to the expression of the enzymes described in connection with alternatives A or B, above.

In another embodiment, the method according to the invention makes use of a photosynthetic microorganism expressing at least the enzymes as described in connection with alternatives A or B, above. Preferably, the microorganism is a photosynthetic bacterium, or a microalgae. In a further embodiment the microorganism is an algae, more preferably an algae belonging to the diatomeae. Even more preferably such a microorganism has the natural or artificial property of endogenously producing crotyl alcohol. In this case the microorganism would be capable of producing butadiene directly from CO₂ present in solution.

In another embodiment, it is possible to use a microorganism which belongs to the group of acetogenic bacteria which are capable of converting CO (or CO₂+H₂) to produce acetyl-CoA via the so-called Wood-Ljungdahl pathway (Köpke et al.; PNAS 10 (2010), 13087-13092). A fermentation process using such microorganisms is known as syngas fermentation. Strictly mesophilic anaerobes such as C. ljungdahlii, C. aceticum, Acetobacterium woodii, C. autoethanogenum, and C. carboxydeviron, are frequently being used in syngas fermentation (Munasingheet et al.; Bioresource Technology 101 (2010), 5013-5022).

It is also conceivable to use in the method according to the invention a combination of (micro)organisms wherein different (micro)organisms express different enzymes as described above. In a further embodiment at least one of the microorganisms is capable of producing crotyl alcohol or, in an alternative embodiment, a further microorganism is used in the method which is capable of producing crotyl alcohol.

In another embodiment the method according to the invention makes use of a multicellular organism expressing at least the enzymes as described in connection with alternatives A or B, above. Examples for such organisms are plants or animals.

In a particular embodiment, the method according to the invention involves culturing microorganisms in standard culture conditions (30-37° C. at 1 atm, in a fermenter allowing aerobic growth of the bacteria) or non-standard conditions (higher temperature to correspond to the culture conditions of thermophilic organisms, for example).

In a further embodiment the method of the invention is carried out under microaerophilic conditions. This means that the quantity of injected air is limiting so as to minimize residual oxygen concentrations in the gaseous effluents containing butadiene.

In another embodiment the method according to the invention furthermore comprises the step of collecting the gaseous butadiene degassing out of the reaction. Thus in a preferred embodiment, the method is carried out in the presence of a system for collecting butadiene under gaseous form during the reaction.

As a matter of fact, butadiene adopts the gaseous state at room temperature and atmospheric pressure. The method according to the invention therefore does not require extraction of butadiene from the liquid culture medium, a step which is always very costly when performed at industrial scale. The evacuation and storage of butadiene and its possible subsequent physical separation and chemical conversion can be performed according to any method known to one of skill in the art and as described above.

In a particular embodiment, the method also comprises detecting butadiene which is present in the gaseous phase. The presence of butadiene in an environment of air or another gas, even in small amounts, can be detected by using various techniques and in particular by using gas chromatography systems with infrared or flame ionization detection, or by coupling with mass spectrometry.

When the process according to the invention is carried out in vivo by using an organism/microorganism providing the respective enzyme activities, the organism, preferably microorganism, is cultivated under suitable culture conditions allowing the occurrence of the enzymatic reaction. The specific culture conditions depend on the specific organism/microorganism employed but are well known to the person skilled in the art. The culture conditions are generally chosen in such a manner that they allow the expression of the genes encoding the enzymes for the respective reactions.

Various methods are known to the person skilled in the art in order to improve and fine-tune the expression of certain genes at certain stages of the culture such as induction of gene expression by chemical inducers or by a temperature shift.

In another embodiment the organism employed in the method according to the invention is a plant. In principle any possible plant can be used, i.e. a monocotyledonous plant or a dicotyledonous plant. It is preferable to use a plant which can be cultivated on an agriculturally meaningful scale and which allows to produce large amounts of biomass. Examples are grasses like Lolium, cereals like rye, wheat, barley, oat, millet, maize, other starch storing plants like potato or sugar storing plants like sugar cane or sugar beet. Conceivable is also the use of tobacco or of vegetable plants such as tomato, pepper, cucumber, egg plant etc. Another possibility is the use of oil storing plants such as rape seed, olives etc. Also conceivable is the use of trees, in particular fast growing trees such as eucalyptus, poplar or rubber tree (Hevea brasiliensis). Particularly preferred is the use of plants which naturally produce crotonaldehyde, e.g. soybeans. Such plants are preferably further modified so as to be able to convert crotonaldehyde into crotyl alcohol.

In another embodiment, the method according to the invention is characterized by the conversion of a carbon source, such as glucose, into crotyl alcohol (preferably via crotonyl-CoA and crotonaldehyde) followed by the conversion of crotyl alcohol into butadiene.

In another embodiment, the method according to the invention comprises the production of butadiene from atmospheric CO₂ or from CO₂ artificially added to the culture medium. In this case the method is implemented in an organism which is able to carry out photosynthesis, such as for example microalgae.

As described above, it is possible to use in the method according to the invention a (micro)organism which is genetically modified so as to contain a nucleic acid molecule encoding at least one of the enzymes as described above in connection with alternatives A or B. Such a nucleic acid molecule encoding an enzyme as described above can be used alone or as part of a vector. The nucleic acid molecules can further comprise expression control sequences operably linked to the polynucleotide comprised in the nucleic acid molecule. The term “operatively linked” or “operably linked”, as used throughout the present description, refers to a linkage between one or more expression control sequences and the coding region in the polynucleotide to be expressed in such a way that expression is achieved under conditions compatible with the expression control sequence.

Expression comprises transcription of the heterologous DNA sequence, preferably into a translatable mRNA. Regulatory elements ensuring expression in fungi as well as in bacteria, are well known to those skilled in the art. They encompass promoters, enhancers, termination signals, targeting signals and the like. Examples are given further below in connection with explanations concerning vectors.

Promoters for use in connection with the nucleic acid molecule may be homologous or heterologous with regard to its origin and/or with regard to the gene to be expressed. Suitable promoters are for instance promoters which lend themselves to constitutive expression. However, promoters which are only activated at a point in time determined by external influences can also be used. Artificial and/or chemically inducible promoters may be used in this context.

The vectors can further comprise expression control sequences operably linked to said polynucleotides contained in the vectors. These expression control sequences may be suited to ensure transcription and synthesis of a translatable RNA in bacteria or fungi.

In addition, it is possible to insert different mutations into the polynucleotides by methods usual in molecular biology (see for instance Sambrook and Russell (2001), Molecular Cloning: A Laboratory Manual, CSH Press, Cold Spring Harbor, N.Y., USA), leading to the synthesis of polypeptides possibly having modified biological properties. The introduction of point mutations is conceivable at positions at which a modification of the amino acid sequence for instance influences the biological activity or the regulation of the polypeptide.

Moreover, mutants possessing a modified substrate or product specificity can be prepared. Preferably, such mutants show an increased activity. Furthermore, the introduction of mutations into the polynucleotides encoding an enzyme as defined above allows the gene expression rate and/or the activity of the enzymes encoded by said polynucleotides to be optimized.

For genetically modifying bacteria or fungi, the polynucleotides encoding an enzyme as defined above or parts of these molecules can be introduced into plasmids which permit mutagenesis or sequence modification by recombination of DNA sequences. Standard methods (see Sambrook and Russell (2001), Molecular Cloning: A Laboratory Manual, CSH Press, Cold Spring Harbor, N.Y., USA) allow base exchanges to be performed or natural or synthetic sequences to be added. DNA fragments can be connected to each other by applying adapters and linkers to the fragments. Moreover, engineering measures which provide suitable restriction sites or remove surplus DNA or restriction sites can be used. In those cases, in which insertions, deletions or substitutions are possible, in vitro mutagenesis, “primer repair”, restriction or ligation can be used. In general, a sequence analysis, restriction analysis and other methods of biochemistry and molecular biology are carried out as analysis methods.

The polynucleotide introduced into a (micro)organism is expressed so as to lead to the production of a polypeptide having any of the activities described above. An overview of different expression systems is for instance contained in Methods in Enzymology 153 (1987), 385-516, in Bitter et al. (Methods in Enzymology 153 (1987), 516-544) and in Sawers et al. (Applied Microbiology and Biotechnology 46 (1996), 1-9), Billman-Jacobe (Current Opinion in Biotechnology 7 (1996), 500-4), Hockney (Trends in Biotechnology 12 (1994), 456-463), Griffiths et al., (Methods in Molecular Biology 75 (1997), 427-440). An overview of yeast expression systems is for instance given by Hensing et al. (Antonie van Leuwenhoek 67 (1995), 261-279), Bussineau et al. (Developments in Biological Standardization 83 (1994), 13-19), Gellissen et al. (Antonie van Leuwenhoek 62 (1992), 79-93, Fleer (Current Opinion in Biotechnology 3 (1992), 486-496), Vedvick (Current Opinion in Biotechnology 2 (1991), 742-745) and Buckholz (Bio/Technology 9 (1991), 1067-1072).

Expression vectors have been widely described in the literature. As a rule, they contain not only a selection marker gene and a replication-origin ensuring replication in the host selected, but also a bacterial or viral promoter, and in most cases a termination signal for transcription. Between the promoter and the termination signal there is in general at least one restriction site or a polylinker which enables the insertion of a coding DNA sequence. The DNA sequence naturally controlling the transcription of the corresponding gene can be used as the promoter sequence, if it is active in the selected host organism. However, this sequence can also be exchanged for other promoter sequences. It is possible to use promoters ensuring constitutive expression of the gene and inducible promoters which permit a deliberate control of the expression of the gene. Bacterial and viral promoter sequences possessing these properties are described in detail in the literature. Regulatory sequences for the expression in microorganisms (for instance E. coli, S. cerevisiae) are sufficiently described in the literature. Promoters permitting a particularly high expression of a downstream sequence are for instance the T7 promoter (Studier et al., Methods in Enzymology 185 (1990), 60-89), lacUV5, trp, trp-lacUV5 (DeBoer et al., in Rodriguez and Chamberlin (Eds), Promoters, Structure and Function; Praeger, New York, (1982), 462-481; DeBoer et al., Proc. Natl. Acad. Sci. USA (1983), 21-25), Ip1, rac (Boros et al., Gene 42 (1986), 97-100). Inducible promoters are preferably used for the synthesis of polypeptides. These promoters often lead to higher polypeptide yields than do constitutive promoters. In order to obtain an optimum amount of polypeptide, a two-stage process is often used. First, the host cells are cultured under optimum conditions up to a relatively high cell density. In the second step, transcription is induced depending on the type of promoter used. In this regard, a tac promoter is particularly suitable which can be induced by lactose or IPTG (=isopropyl-β-D-thiogalactopyranoside) (deBoer et al., Proc. Natl. Acad. Sci. USA 80 (1983), 21-25). Termination signals for transcription are also described in the literature.

The transformation of the host cell with a polynucleotide or vector according to the invention can be carried out by standard methods, as for instance described in Sambrook and Russell (2001), Molecular Cloning: A Laboratory Manual, CSH Press, Cold Spring Harbor, N.Y., USA; Methods in Yeast Genetics, A Laboratory Course Manual, Cold Spring Harbor Laboratory Press, 1990. The host cell is cultured in nutrient media meeting the requirements of the particular host cell used, in particular in respect of the pH value, temperature, salt concentration, aeration, antibiotics, vitamins, trace elements etc.

The present invention also relates to an organism, preferably a microorganism, which is able to express the enzymes required for the conversion of crotyl alcohol into butadiene according to alternative A or B of the method of the invention (according to the first aspect) as described above and which is able to convert crotyl alcohol into butadiene.

Thus, the present invention also relates to a (micro)organism which expresses

• A) (a) (i) a hydroxyethylthiazole kinase (EC 2.7.1.50); or
  • (ii) a thiamine kinase (EC 2.7.1.89); and
•  (b) (i) a terpene synthase, e.g. an isoprene synthase (EC 4.2.3.27); or
  • (ii) an isopentenyl phosphate kinase and a terpene synthase, e.g. an isoprene synthase (EC 4.2.3.27); or
• B) (a) (i) a 2-amino-4-hydroxy-6-hydroxymethyldihydropteridine diphosphokinase (EC 2.7.6.3); or
  • (ii) a thiamine diphosphokinase (EC 2.7.6.2); and
•  (b) a terpene synthase, e.g. an isoprene synthase (EC 4.2.3.27), and which is capable of converting crotyl alcohol into butadiene. As regards preferred embodiments, the same applies as has been set forth above in connection with the method according to the invention.

As regards in particular the terpene synthase and the preferred embodiments of terpene synthases to be expressed by the (micro)organism, the same applies as has been set forth above in connection with the method according to the invention.

Thus, in one preferred embodiment the terpene synthase is

(a) an isoprene synthase (EC 4.2.3.27); or
(b) a myrcene/ocimene synthase (EC 4.2.3.15); or
(c) a farnesene synthase (EC 4.2.3.46 or EC 4.2.3.47); or
(d) a pinene synthase (EC 4.2.3.14); or
(e) a monoterpene synthase.

The present invention also relates to an organism, preferably a microorganism, which is able to express the enzymes required for the conversion of crotonyl-CoA into crotonaldehyde and/or crotyl alcohol as described in connection with the second aspect of the invention. Thus, the present invention also relates to a (mirco)organism which expresses

(i) a hydroxymethylglutaryl-CoA reductase (EC 1.1.1.34); and/or
(ii) an acetaldehyde dehydrogenase (EC 1.2.1.10); and/or
(iii) an alcohol dehydrogenase (EC 1.1.1.1); and/or
(iv) an aldehyde/alcohol dehydrogenase; and/or
(v) an acyl-CoA reductase; and/or
(vi) an aldo-keto reductase (AKR); and/or
(vii) an aldehyde reductase; and/or
(viii) a short-chain dehydrogenase/fatty acyl-CoA reductase
(ix) and which is capable of converting crotonyl-CoA into crotonaldehyde and/or crotyl alcohol.

The present invention also relates to an organism, preferably a microorganism, which is further able to express the enzymes required for the conversion of 3-hydroxybutyryl-CoA into crotonyl-CoA. Thus, the present invention also relates to a (mirco)organism which expresses a 3-hydroxybutyryl-CoA dehydratase (EC 4.2.1.55) and/or an enoyl-CoA hydratase (EC 4.2.1.17) and/or an enoyl-CoA hydratase 2 (EC 4.2.1.119) and/or a crotonyl-[acyl-carrier-protein] hydratase (EC 4.2.1.58) and which is capable of converting 3-hydroxybutyryl-CoA into crotonyl-CoA.

The present invention also relates to an organism, preferably a microorganism, which is further able to express the enzymes required for the conversion of acetoacetyl-CoA into 3-hydroxybutyryl-CoA. Thus, the present invention also relates to a (mirco)organism which further expresses an acetoacetyl-CoA reductase (EC 1.1.1.36) and which is capable of converting acetoacetyl-CoA into 3-hydroxybutyryl-CoA.

Finally, the present invention also relates to an organism, preferably a microorganism, which is further able to express the enzymes required for the enzymatic production of acetoacetyl-CoA. This production may be achieved by the conversion of acetyl-CoA into acetoacetyl-CoA or by the conversion of acetyl-CoA and malonyl-CoA into acetoacetyl-CoA. Thus, the present invention also relates to a (mirco)organism which further expresses an acetyl-CoA C-acetyltransferase (EC 2.3.1.9) and which is capable of converting acetyl-CoA into acetoacetyl-CoA and/or which further expresses a acetoacetyl-CoA synthase and which is capable of converting acetyl-CoA and malonyl-CoA into acetoacetyl-CoA.

In one embodiment an organism according to the present invention is a recombinant organism in the sense that it is genetically modified due to the introduction of at least one nucleic acid molecule encoding at least one of the above mentioned enzymes. Preferably such a nucleic acid molecule is heterologous with regard to the organism which means that it does not naturally occur in said organism.

The microorganism is preferably a bacterium, a yeast or a fungus. In another preferred embodiment the organism is a plant or non-human animal. As regards other preferred embodiments, the same applies as has been set forth above in connection with the method according to the invention.

In an embodiment according to the present invention in which an organism, preferably a microorganism, is employed which is capable of providing crotonyl-CoA, such a (micro)organism is advantageously further genetically modified so as to avoid diverting of the crotonyl-CoA into other pathways. It is known, for example, that crotonyl-CoA can be reduced by a variety of enzymes to lead to butyryl-CoA. These enzymes generally belong to the EC classification EC 1.3.1 and include acyl-CoA dehydrogenase (NADP⁺, EC 1.3.1.8), enoyl-[acyl-carrier-protein] reductase (NADH; EC 1.3.1.9), enoyl-[acyl-carrier-protein] reductase (NADPH; EC 1.3.1.10), cis-2-enoyl-CoA reductase (NADPH; EC 1.3.1.37) and trans-2-enoyl-CoA reductase (NADPH; EC 1.3.1.38). Thus, in one embodiment the organism is genetically modified so as to decrease the activity of enzymes which may lead to a reduction of crotonyl-CoA to butyryl-CoA and thus to a diversion of crotonyl-CoA into other pathways. Such a reduction of activity can be achieved by methods known to the person skilled in the art and include, for example, the decrease of the expression of the respective gene(s) coding for the respective enzyme(s) by known methods such as antisense approaches, siRNA approaches or the like. In case the respective enzyme activity is not necessary for survival of the microorganism, it can also be knocked out completely, e.g. by disrupting the gene or completely deleting the gene.

The present invention also relates to a composition comprising

• A) (a) (i) a hydroxyethylthiazole kinase (EC 2.7.1.50); or
  • (ii) a thiamine kinase (EC 2.7.1.89); and
•  (b) (i) a terpene synthase, e.g. an isoprene synthase (EC 4.2.3.27); or
  • (ii) an isopentenyl phosphate kinase and a terpene synthase, e.g. an isoprene synthase (EC 4.2.3.27); or
• B) (a) (i) a 2-amino-4-hydroxy-6-hydroxymethyldihydropteridine diphosphokinase EC 2.7.6.3); or
  • (ii) a thiamine diphosphokinase (EC 2.7.6.2); and
•  (b) a terpene synthase, e.g. an isoprene synthase (EC 4.2.3.27).

Such a composition may also comprise crotyl alcohol. As regards preferred embodiments, the same applies as has been set forth above in connection with the method according to the invention.

As regards in particular the terpene synthase and the preferred embodiments of terpene synthases to be expressed by the (micro)organism, the same applies as has been set forth above in connection with the method according to the invention.

Thus, in one preferred embodiment the terpene synthase is

(f) an isoprene synthase (EC 4.2.3.27); or
(g) a myrcene/ocimene synthase (EC 4.2.3.15); or
(h) a farnesene synthase (EC 4.2.3.46 or EC 4.2.3.47); or
(i) a pinene synthase (EC 4.2.3.14); or
(i) a monoterpene synthase.

The present invention also relates to a composition comprising

(i) a hydroxymethylglutaryl-CoA reductase (EC 1.1.1.34); and/or
(ii) an acetaldehyde dehydrogenase (EC 1.2.1.10); and/or
(iii) an alcohol dehydrogenase (EC 1.1.1.1); and/or
(iv) an aldehyde/alcohol dehydrogenase; and/or
(v) an acyl-CoA reductase; and/or
(vi) an aldo-keto reductase (AKR); and/or
(vii) an aldehyde reductase; and/or
(viii) a short-chain dehydrogenase/fatty acyl-CoA reductase.

Moreover, the present invention also relates to such a composition which further comprises a 3-hydroxybutyryl-CoA dehydratase (EC 4.2.1.55) and/or an enoyl-CoA hydratase (EC 4.2.1.17) and/or an enoyl-CoA hydratase 2 (EC 4.2.1.119) and/or a crotonyl-[acyl-carrier-protein] hydratase (EC 4.2.1.58). The present invention also relates to a composition which also comprises an acetoacetyl-CoA reductase (EC 1.1.1.36). Finally, the present invention also relates to a composition which also comprises an acetyl-CoA C-acetyltransferase (EC 2.3.1.9) or an acetoacetyl-CoA synthase.

The present invention also relates to the use of a combination of enzymes comprising:

• A) (a) (i) a hydroxyethylthiazole kinase (EC 2.7.1.50); or
  • (ii) a thiamine kinase (EC 2.7.1.89); and
•  (b) (i) a terpene synthase, e.g. an isoprene synthase (EC 4.2.3.27); or
  • (ii) an isopentenyl phosphate kinase and a terpene synthase, e.g. an isoprene synthase (EC 4.2.3.27); or
• B) (a) (i) a 2-amino-4-hydroxy-6-hydroxymethyldihydropteridine diphosphokinase EC 2.7.6.3); or
  • (ii) a thiamine diphosphokinase (EC 2.7.6.2); and
•  (b) a terpene synthase, e.g. an isoprene synthase (EC 4.2.3.27);
  for the production of butadiene from crotyl alcohol. As regards preferred embodiments, the same applies as has been set forth above in connection with the method according to the invention.

As regards in particular the terpene synthase and the preferred embodiments of terpene synthases to be expressed by the (micro)organism, the same applies as has been set forth above in connection with the method according to the invention.

Thus, in one preferred embodiment the terpene synthase is

(k) an isoprene synthase (EC 4.2.3.27); or
(l) a myrcene/ocimene synthase (EC 4.2.3.15); or
(m) a farnesene synthase (EC 4.2.3.46 or EC 4.2.3.47); or
(n) a pinene synthase (EC 4.2.3.14); or
(o) a monoterpene synthase.

The present invention also relates to the use of

(i) a hydroxymethylglutaryl-CoA reductase (EC 1.1.1.34); and/or
(ii) an acetaldehyde dehydrogenase (EC 1.2.1.10); and/or
(iii) an alcohol dehydrogenase (EC 1.1.1.1); and/or
(iv) an aldehyde/alcohol dehydrogenase; and/or
(v) an acyl-CoA reductase; and/or
(vi) an aldo-keto reductase (AKR); and/or
(vii) an aldehyde reductase; and/or
(viii) a short-chain dehydrogenase/fatty acyl-CoA reductase
for the conversion of crotonyl-CoA into crotonaldehyde and/or crotyl alcohol.

Furthermore the present invention also relates to the use of a combination of enzymes comprising

(a) an acetoacetyl-CoA reductase (EC 1.1.1.36); and
(b) (i) a 3-hydroxybutyryl-CoA dehydratase (EC 4.2.1.55); and or

• • (ii) an enoyl-CoA hydratase (EC 4.2.1.17); and/or
  • (iii) an enoyl-CoA hydratase 2 (EC 4.2.1.119); and/or
  • (iv) a crotonyl-[acyl-carrier-protein] hydratase (EC 4.2.1.58)
    for the production of crotonyl-CoA from acetoacetyl-CoA.

The present invention also relates to the use of a combination of enzymes comprising

(a) (i) an acetyl-CoA C-acetyltransferase (EC 2.3.1.9) and/or

• • (ii) an acetoacetyl-CoA synthase; and
    (b) an acetoacetyl-CoA reductase (EC 1.1.1.36);
    (c) (i) a 3-hydroxybutyryl-CoA dehydratase (EC 4.2.1.55); and/or
  • (ii) an enoyl-CoA hydratase (EC 4.2.1.17); and/or
  • (iii) an enoyl-CoA hydratase 2 (EC 4.2.1.119); and/or
  • (iv) a crotonyl-[acyl-carrier-protein] hydratase (EC 4.2.1.58)
    for the production of crotonyl-CoA from acetyl-CoA.

FIG. 1 shows the chemical structure of crotonyl alcohol.

FIG. 2 shows the chemical structure of crotyl phosphate. and crotyl diphosphate

FIG. 3 shows the chemical structure of crotonaldehyde.

FIG. 4 shows the chemical structure of butadiene.

FIG. 5 shows a scheme of the ADP quantification assay, monitoring NADH consumption by the decrease of absorbance at 340 nm.

FIG. 6 shows a mass spectrum of an enzymatic assay with hydroxyethylthiazole kinase from E. coli.

FIG. 7 shows a mass spectrum of a control assay without enzyme.

FIG. 8 shows a comparison between dimethylallyl diphosphate and crotyl diphosphate and their conversion into isoprene (2-methyl-buta-1,3-diene) and butadiene, respectively.

FIG. 9 shows the formula of crotonyl-Coenzyme A

FIG. 10 shows the MS spectrum of the trans crotyl monophosphate phosphorylation reaction catalyzed by isopentenyl monophosphate kinase from M. jannaschii (a) and of a control assay without enzyme (b).

FIG. 11 shows 1,3-butadiene production from trans crotyl monophosphate catalyzed by terpene synthases.

FIG. 12 shows the mass spectrum of commercial 1,3-butadiene (a) and 1,3-butadiene produced from trans crotyl monophosphate in an enzymatic reaction catalyzed by monoterpene synthase from E. globulus (b).

FIG. 13 shows 1,3-butadiene production from trans crotyl diphosphate catalyzed by terpene synthases.

FIG. 14 shows a time courses of NADPH oxidation in crotonyl-CoA reduction assay with reductase from Hahella chejuensis and varying concentrations of NADPH.

FIG. 15 shows a chromatogram of the crotonyl-CoA reduction reaction catalyzed by acyl-CoA reductase from H. chejuensis.

Other aspects and advantages of the invention will be described in the following examples, which are given for purposes of illustration and not by way of limitation.

EXAMPLES

Example 1

Cloning, Expression and Purification of Enzymes

Cloning, Bacterial Cultures and Expression of Proteins

The genes encoding studied enzymes were cloned in pET 25b vector (Novagen). A stretch of 6 histidine codons was inserted after the methionine initiation codon to provide an affinity tag for purification. Competent E. coli BL21(DE3) cells (Novagen) were transformed with these vectors according to the heat shock procedure. The transformed cells were grown with shaking (160 rpm) on ZYM-5052 auto-induction medium (Studier F W, Prot. Exp. Pur. 41 (2005), 207-234) for 6 h at 37° C. and protein expression was continued at 28° C. or 20° C. overnight (approximately 16 h). The cells were collected by centrifugation at 4° C., 10,000 rpm for 20 min and the pellets were frozen at −80° C.

Protein Purification and Concentration

The pellets from 200 ml of culture cells were thawed on ice and resuspended in 5 ml of Na₂HPO₄ pH 8 containing 300 mM NaCl, 5 mM MgCl₂ and 1 mM DTT. Twenty microliters of lysonase (Novagen) were added. Cells were incubated 10 minutes at room temperature and then returned to ice for 20 minutes. Cell lysis was completed by sonication for 3×15 seconds. The bacterial extracts were then clarified by centrifugation at 4° C., 10,000 rpm for 20 min. The clarified bacterial lysates were loaded on PROTINO-1000 Ni-TED column (Macherey-Nagel) allowing adsorption of 6-His tagged proteins. Columns were washed and the enzymes of interest were eluted with 4 ml of 50 mM Na₂HPO₄ pH 8 containing 300 mM NaCl, 5 mM MgCl₂, 1 mM DTT, 250 mM imidazole. Eluates were then concentrated and desalted on Amicon Ultra-4 10 kDa filter unit (Millipore) and resuspended in 0.25 ml 50 mM Tris-HCl pH 7.4 containing 0.5 mM DTT and 5 mM MgCl₂. Protein concentrations were quantified according to the Bradford method. The purity of proteins thus purified varied from 50% to 90%.

Example 2

Screening for Crotyl Alcohol Phosphorylation Activity

The release of ADP that is associated with crotyl alcohol phosphorylation was quantified using the pyruvate kinase/lactate dehydrogenase coupled assay (FIG. 5). The purified 4-methyl-5-(2-hydroxyethyl)thiazole kinases from Escherichia coli (SEQ ID NO:2), Bacillus subtilis (SEQ ID NO:1), Rhizobium leguminosarum (SEQ ID NO:3) were evaluated for their ability to phosphorylate crotyl alcohol releasing ADP. The studied enzymatic reaction was carried out under the following conditions at 37° C.:

50 mM Tris-HCl pH 7.5

10 mM MgCl₂

100 mM KCl

5 mM ATP

0.4 mM NADH

1 mM Phosphoenolpyruvate

3 U/ml Lactate dehydrogenase
1.5 U/ml Pyruvate kinase
50 mM crotyl alcohol, mixture cis and trans
The pH was adjusted to 7.5

Each assay was started by addition of a particular enzyme at a concentration 0.05 mg/ml and the disappearance of NADH was monitored by following the absorbance at 340 nM.

Assays with hydroxyethylthiazole kinase from the E. coli and Rh. leguminosarum gave rise to a reproducible and significant increase in ADP production in the presence of crotyl alcohol (Table 1). Mass spectrometry was then used to verify the formation of crotyl monophosphate in the assay with the E. coli enzyme.

TABLE 1
4-methyl-5-(2-hydroxyethyl) Activity, micromole/
thiazole kinase             min · mg protein
E. coli                     0.220
Rh. leguminosarum           0.087
B. subtilis                 0.014

Example 3

Mass Spectrometry Analysis of the Crotyl Alcohol Phosphorylation Reaction

The desired enzymatic reactions were carried out under the following conditions:

50 mM Tris-HCl pH7.5

10 mM MgCl2

50 mM cis or trans crotyl alcohol

20 mM ATP

0.1 mg/ml purified hydroxythiazole kinase from E. coli (SEQ ID NO:2)

The control reactions without enzyme, without substrate and without ATP were run in parallel. The assays were incubated overnight without shaking at 37° C. Typically, an aliquot of 2001 reaction was removed, centrifuged and the supernatant was transferred into a clean vial. The MS spectra were obtained on an ion trap mass spectrometer (Esquire 3000, Bruker) in negative ion mode by direct injection of the sample using a syringe pump operated at a flow rate of 2 ml/h. The presence of crotyl monophosphate was evaluated. MS analysis showed an [M-H]− ion at m/z 151, corresponding to crotyl monophosphate, from the enzymatic sample but not from the controls (FIGS. 6 and 7).

Example 4

Screening for 1,3-Butadiene Production from Crotyl Monophosphate Using Purified Isoprene Synthases

Crotyl monophosphate is synthesized upon request by a company specialized in custom synthesis (Syntheval, France).

The enzymatic assays are carried out under the following conditions at 37° C.:

50 mM Tris-HCl pH7.5

1 to 200 mM cis or trans crotyl monophosphate

1 mM DTT

1 to 20 mM MgCl₂

1 to 5 mg/ml isoprene synthase

The enzyme-free control reaction is carried out in parallel. The enzymatic mixture is incubated at 37° C. for 72 h in a sealed vial (Interchim).

Volatile compounds in the headspace of the reaction mixture are collected using a gas syringe equipped with an anti-backup mechanism and are directly injected into a GC-430 gas chromatograph (Brucker) equipped with an FID detector and a GAS-PRO column (Agilent). The enzymatic reaction product is identified by direct comparison with standard 1,3-butadiene (Sigma).

The identity of the gas is further confirmed in GC/MS analyses.

Example 5

Screening for Crotyl Monophosphate Phosphorylation Activity

Sequences of isopentenyl monophosphate kinases inferred from the genomes of several members of the Archaea, in particular Methanothermobacter (SEQ ID NO:5), Methanocaldococcus (SEQ ID NO:6) and Thermoplasma (SEQ ID NO:4) genus, are generated by oligonucleotide concatenation to fit the codon usage of E. coli. A stretch of 6 histidine codons is inserted after the methionine initiation codon to provide an affinity tag for purification. The genes thus synthesized are cloned in a pET25b expression vector and the proteins are produced according to the protocol described in Example 1. The enzymes are then assayed using the method described in Example 2 with crotyl monophosphate concentrations varying from 0 to 50 mM. The release of ADP that is associated with crotyl monophosphate phosphorylation is quantified using the pyruvate kinase/lactate dehydrogenase coupled assay. Each assay is started by addition of particular enzyme (at a final concentration from 0.05 mg/ml to 1 mg/ml) and the disappearance of NADH is monitored by following the absorbance at 340 nM.

Example 6

Mass Spectrometry Analysis of the Crotyl Monophosphate Phosphorylation Reaction

Enzymatic assays are run in 50 mM Tris-HCl pH 7.5, contained 5 mM MgCl₂, 20 mM ATP, 2 mM β-mercaptoethanol and crotyl monophosphate varying in the range from 0 to 50 mM in a final volume of 0.25 ml. The reactions are initiated with the addition of purified isoprenol monophosphate kinase and incubated overnight at 37-55° C. The control reactions contain no enzyme. Following incubation samples are processed by mass spectrometry analysis. An aliquot of 200 μl reaction is removed, centrifuged and the supernatant is transferred to a clean vial. The MS spectra are obtained on ion trapp mass spectrometer (Esquire 3000, Bruker) in negative ion mode by direct injection of sample using a syringe pump operated at a flow rate of 2 ml/h.

Example 7

Screening for 1,3-Butadiene Production from Crotyl Diphosphate Using Purified Isoprene Synthases

Crotyl diphosphate is synthesized upon request by a company specialized in custom synthesis, Syntheval (France).

The enzymatic assays are carried out under the following conditions at 37° C.:

50 mM Tris-HCl pH7.5

1 to 200 mM cis or trans crotyl diphosphate

1 mM DTT

1 to 20 mM MgCl₂

1 to 5 mg/ml isoprene synthase

The enzyme-free control reaction is carried out in parallel. The enzymatic mixture is incubated at 37° C. for 72 h in a sealed vial (Interchim).

Volatile compounds in the headspace of the reaction mixture are collected using a gas syringe equipped with an anti-backup mechanism and are directly injected into a GC-430 gas chromatograph (Brucker) equipped with an FID detector and a GAS-PRO column (Agilent). The enzymatic reaction product is identified by direct comparison with standard 1,3-butadiene (Sigma).

The identity of the gas is further confirmed in GC/MS analyses.

Example 8

Screening of Hydroxymethylglutaryl-CoA (Hmg-CoA) Reductases Using Crotonyl-CoA as a Substrate

Sequences of hydroxymethylglutaryl-CoA reductases inferred from the genomes of prokaryotic and eukaryotic organisms are generated to fit the codon usage of E. coli. A stretch of 6 histidine codons is inserted after the methionine initiation codon to provide an affinity tag for purification. The genes thus synthesized are cloned in a pET25b expression vector and the proteins are produced according to the protocol described in Example 1. The reductase activity of the purified enzymes using crotonyl-CoA as a substrate is then determined by measuring the initial decrease in absorbance at 340 nm due to the NADPH oxidation. The standard assay is performed at pH 7.5, 50 mM phosphate buffer, containing 10 mM dithiothreitol, 0.1 mM NADPH and crotonyl-CoA at concentration varying from 0 to 10 mM.

Example 9

Kinetic Parameters of Crotyl Alcohol Phosphorylation

Kinetic parameters of crotyl alcohol phosphorylation were determined using the spectrophotometric assay described in Example 2. Kinetic parameters obtained for purified 4-methyl-5-(2-hydroxyethyl)thiazole kinase from E. coli are presented in Table 2.

	TABLE 2
		Kinetic parameters
	Substrate	Km, mM	kcat, s−1
	Cis crotyl alcohol	13.6	0.19
	Trans crotyl alcohol	30	0.11

Example 10

Mass Spectrometry Analysis of the Crotyl Monophosphate Phosphorylation Reaction

The enzymatic reactions were carried out under the following conditions:

50 mM Tris-HCl pH 7.5

10 mM MgCl₂

100 mM KCl

50 mM trans crotyl monophosphate

20 mM ATP

0.1 mg/ml purified isopentenyl monophosphate kinase

Control assays were performed in which either no enzyme was added, or no substrate was added. The assays were incubated overnight without shaking at 37° C. Typically, an aliquot of 200 μl reaction was removed, centrifuged and the supernatant was transferred into a clean vial. The MS spectra were obtained on ion trap mass spectrometer (Esquire 3000, Bruker) in negative ion mode by direct injection of sample using a syringe pump operated at a flow rate of 2 ml/h. The presence of crotyl diphosphate was evaluated. MS analysis showed an [M-H]⁻ ion at m/z 231.5, corresponding to crotyl diphosphate, from the enzymatic samples but not from the controls. Examples of mass spectrums of enzymatic assay with isopentenyl monophosphate kinase from M. jannaschii and control assay without enzyme are shown in FIGS. 10a and 10b.

Example 11

Kinetic Parameters of the Crotyl Monophosphate Phosphorylation Reaction

Cis crotyl monophosphate and trans crotyl monophosphate were synthesized upon request by a company specialized in custom synthesis (Syntheval, France). Kinetic parameters for the phosphorylation of these substrates were determined using the spectrophotometric assay described in Example 2. Kinetic parameters obtained with purified isopentenyl monophosphate kinases from different members of the Archaea kingdom are presented in Table 3 (cis crotyl monophosphate as a substrate) and Table 4 (trans crotyl monophosphate as a substrate).

	TABLE 3
	Isopentenyl
	monophosphate	Kinetic parameters
	kinase	Km, mM	kcat, s−1
	Methanocaldococcus	0.20	3.4
	jannaschii
	Methanothermobacter	0.94	5.7
	thermautotrophicus
	Thermoplasma	0.61	1.8
	acidophilum

	TABLE 4
		Kinetic parameters
	Enzyme	Km, mM	kcat, s−1
	Methanocaldococcus	0.49	3.0
	jannaschii
	Methanothermobacter	0.45	8.7
	thermautotrophicus
	Thermoplasma	1	2.2
	acidophilum

Example 12

Enzyme Catalyzed Production of 1,3-Butadiene from Trans Crotyl Monophosphate with Purified Terpene Synthases

The enzymatic assays were carried out under the following conditions at 37° C.:

50 mM Tris-HCl pH 7.5

25 mM trans crotyl monophosphate

2 mM DTT

50 mM MgCl₂

50 mM KCl

2 mg of the purified terpene synthase was added to 0.5 ml of reaction mixture. An enzyme-free control reaction was carried out in parallel. Assays were incubated at 37° C. for 24 h in a sealed vial of 1.5 ml (Interchim) with shaking.

One ml of the gaseous phase was then collected and directly injected into a Varian GC-430 gas chromatograph equipped with a flame ionization detector (FID). Nitrogen was used as carrier gas with a flow rate of 1.5 ml/min. Volatile compounds were chromatographically separated on RT-Alumina Bond/Na₂SO₄ column (Restek) using an isothermal mode at 130° C. The enzymatic reaction product was identified by direct comparison with 1,3-butadiene standard (Sigma). Several terpene synthases were shown to catalyze butadiene production from trans crotyl monophosphate (FIG. 11).

Gas chromatography-mass spectrometry was then used to confirm the identity of the product detected by GC/FID. Assay with E. globulus enzyme (SEQ ID NO: 8) was analyzed on a Varian 3400Cx gas chromatograph equipped with Varian Saturn 3 mass selective detector. A mass spectrum of 1,3-butadiene obtained by enzymatic conversion of trans crotyl monophosphate was similar to that of commercial 1,3-butadiene (FIGS. 12a and 12b).

Example 13

Kinetic Parameters of Enzyme Catalyzed Production of 1,3-Butadiene from Trans Crotyl Monophosphate

The kinetic parameters of enzyme catalyzed production of 1,3-butadiene from trans crotyl monophosphate were measured under the following conditions:

50 mM Tris-HCl pH 7.5

20 mM MgCl₂

20 mM KCl

2 mM DTT

0-25 mM trans crotyl monophosphate

The reaction was initiated by addition of 0.25 mg of purified monoterpene synthase from Eucalyptus globulus to 0.5 ml of reaction mixture. An enzyme-free control reaction was carried out in parallel. Assays were incubated at 37° C. for 0.5-4 h in a sealed vial of 1.5 ml (Interchim) with shaking.

1,3-butadiene production was analyzed using the GC/FID procedure described in Example 12. Monoterpene synthase from E. globulus was found to have a K_M value of 6 mM and a k_cat of at least 0.2×10⁻⁵ sec⁻¹.

Example 14

Enzyme Catalyzed Production of 1,3-Butadiene from Trans Crotyl Diphosphate with Purified Terpene Synthases

The enzymatic assays were carried out under the following conditions at 37° C.:

50 mM Tris-HCl pH 7.5

25 mM trans crotyl diphosphate

2 mM DTT

50 mM MgCl₂

50 mM KCl

2 mg of the purified terpene synthase was added to 0.5 ml of reaction mixture. An enzyme-free control reaction was carried out in parallel. Assays were incubated at 37° C. for 24 h in a sealed vial of 1.5 ml (Interchim) with shaking.

One ml of the gaseous phase was then collected and directly injected into a Varian GC-430 gas chromatograph equipped with a flame ionization detector (FID). Nitrogen was used as carrier gas with a flow rate of 1.5 ml/min. Volatile compounds were chromatographically separated on RT-Alumina Bond/Na₂SO₄ column (Restek) using an isothermal mode at 130° C. The enzymatic reaction product was identified by direct comparison with 1,3-butadiene standard (Sigma). Several terpene synthases were shown to catalyze butadiene production from trans crotyl diphosphate (FIG. 13).

Example 15

Kinetic Parameters of Enzyme Catalyzed Production of 1,3-Butadiene from Trans Crotyl Diphosphate

The kinetic parameters of enzyme catalyzed production of 1,3-butadiene from trans crotyl monophosphate were measured under the following conditions:

50 mM Tris-HCl pH 7.5

20 mM MgCl₂

20 mM KCl

2 mM DTT

0-25 mM trans crotyl diphosphate

The reaction was initiated by addition of 0.25 mg of purified monoterpene synthase from Eucalyptus globulus to 0.5 ml of reaction mixture. An enzyme-free control reaction was carried out in parallel. Assays were incubated at 37° C. for 0.5-4 h in a sealed vial of 1.5 ml (Interchim) with shaking.

1,3-butadiene production was analyzed using the GC/FID procedure described in Example 12. Monoterpene synthase from E. globulus was found to have a K_M value of 7 mM and a k_cat of at least 0.3×10⁻⁴ sec⁻¹.

Example 16

Screening of Short-Chain Dehydrogenases/Reductases with Crotonyl-CoA as Substrate

Sequences of short-chain dehydrogenases/reductases inferred from the genomes of prokaryotic organisms were generated by oligonucleotide concatenation to fit the codon usage of E. coli. A stretch of 6 histidine codons is inserted after the methionine initiation codon to provide an affinity tag for purification. The genes thus synthesized were cloned in a pET25b expression vector and the proteins were produced according to the protocol described in Example 1.

For the reductase assay, a reaction mixture containing 50 mM potassium phosphate pH 7.5, 0.1-0.4 mM NADPH, 100 mM NaCl, 5 mM trans crotonyl-CoA and 0.5-1 mg/ml enzyme in a total volume of 120 μl was used and the reaction was carried out at 37° C. for 20 min. Control assays were performed in which either no enzyme was added, or no substrate was added. Each sample was continuously monitored for the decrease of NADPH at 340 nm on a SpectraMax Plus384 UV/Vis Microplate Reader (Molecular Device). Several enzymes demonstrated crotonyl-CoA reductase activity with NADPH as co-substrate (FIG. 14 which shows a time courses of NADPH oxidation in crotonyl-CoA reduction assay with reductase from Hahella chejuensis (SEQ ID NO: 17) and varying concentrations of NADPH, Table 5).

TABLE 5
                                 Activity,
                                 μmol/min/mg
Enzyme                           protein
Short-chain dehydrogenase/reductase 1.4
(Fatty alcohol forming acyl-CoA reductase)
from Marinobacter
aquaeolei VT8 (SEQ ID NO: 13)
Short chain alcohol dehydrogenase- 7.5
like protein from
Marinobacter manganoxydans
(SEQ ID NO: 14)
Short chain alcohol dehydrogenase- 4
like protein from
Marinobacter algicola
(SEQ ID NO: 16)
Short chain alcohol dehydrogenase- 4.9
like protein from
Hahella chejuensis
Short chain alcohol dehydrogenase- 1.2
like protein from
Marinobacter
sp. ELB17 (SEQ ID NO: 15)

The products of enzymatic reduction of crotonyl-CoA were next analyzed by high-performance liquid chromatography (HPLC).

Example 17

HPLC Studies of Enzymatic Reduction of Crotonyl-CoA

The enzymatic assays were carried out under the following conditions:

50 mM Potassium phosphate pH 7.5

100 mM KCl

24 mM trans crotonyl-CoA

80 mM NADPH

The reactions were initiated by addition of 150 μg of purified dehydrogenase/reductase to 150 μl of reaction mixture. Assays were incubated at 37° C. for 0.5-6 h. The reactions were stopped by heating at 65° C. for 5 minutes, reaction mixtures were centrifuged and 120 μl of the clarified supernatant were transferred into a clean vial. The reaction products were then extracted with an equal volume of ethyl acetate. 100 μl of the upper ethyl acetate phase was transferred into a clean vial for HPLC analysis. Commercial crotonaldehyde and crotyl alcohol were used as reference. HPLC-UV analysis was performed using a 1260 Inifinity LC System (Agilent). 10 μl of samples were separated on Zorbax SB-Aq column (250×4.6 mm, 3.5 μm particle size) with a mobile phase flow rate of 1.5 ml/min. The mobile phase consisted of 95:5 (v/v) H₂O/Acetonitrile containing 8.4 mM sulfuric acid. Retention time for trans crotyl alcohol and crotonaldehyde in these conditions were 4.3 and 5.4 min, respectively.

The HPLC analysis showed that crotonaldehyde and crotyl alcohol were formed by enzyme catalyzed reduction of crotonyl-CoA. A typical chromatogram obtained with short chain alcohol dehydrogenase-like protein from H. chejuensis is shown on FIG. 15.

These data indicate that the short-chain dehydrogenase/reductase catalyzes the four-electron reduction of crotonyl-CoA to crotyl alcohol via the aldehyde intermediate.

Example 18

Kinetic Parameters of Crotyl Alcohol Production from Trans Crotonyl-CoA

Kinetic parameters values towards NADPH were determined at fixed concentration of crotonyl-CoA (5 mM) and varying NADPH concentration from 0 to 0.8 mM. NADPH oxidation was measured spectrophotometrically at 340 nm according to the procedure described in Example 16.

The short chain alcohol dehydrogenase-like protein from H. chejuensis was found to have a K_M of 1 mM and a k_cat of 6.0 sec⁻¹ towards NADPH as substrate.

Kinetic parameters values towards crotonyl-CoA were determined at fixed concentration of NADPH (80 mM) and varying crotonyl-CoA concentration from 0 to 32 mM. Kinetic parameters for the overall reaction were determined by crotyl alcohol quantification using HPLC procedure described in Example 17. The short chain alcohol dehydrogenase-like protein from H. chejuensis was found to have a K_M of 5 mM and a k_cat of at least 0.05 sec⁻¹.

Claims

1. A method for the production of butadiene comprising the enzymatic conversion of crotyl alcohol into butadiene via crotyl phosphate or crotyl diphosphate.

2. The method of claim 1 comprising the steps of,

(i) enzymatically converting crotyl alcohol into crotyl phosphate; and

(ii) enzymatically converting crotyl phosphate into butadiene.

3. The method of claim 2 wherein step (ii) consists of a single enzymatic reaction in which crotyl phosphate is directly converted into butadiene.

4. The method of claim 3 wherein the enzymatic conversion of crotyl phosphate into butadiene is achieved by the use of a terpene synthase.

5. The method of claim 4 wherein the terpene synthase is

(a) an isoprene synthase (EC 4.2.3.27); or

(b) a myrcene/ocimene synthase (EC 4.2.3.15); or

(c) a farnesene synthase (EC 4.2.3.46 or EC 4.2.3.47); or

(d) a pinene synthase (EC 4.2.3.14); or

(e) a monoterpene synthase.

6. The method of claim 2 wherein step (ii) consists of two enzymatic reactions comprising:

(a) the enzymatic conversion of crotyl phosphate into crotyl diphosphate; and

(b) the enzymatic conversion of crotyl diphosphate into butadiene.

7. The method of claim 6 wherein the enzymatic conversion of crotyl phosphate into crotyl diphosphate is achieved by the use of an isopentenyl phosphate kinase.

8. The method of claim 6 wherein the enzymatic conversion of crotyl diphosphate into butadiene is achieved by the use of a terpene synthase

9. The method of claim 8 wherein the terpene synthase is

(a) an isoprene synthase (EC 4.2.3.27); or

(b) a myrcene/ocimene synthase (EC 4.2.3.15); or

(c) a farnesene synthase (EC 4.2.3.46 or EC 4.2.3.47); or

(d) a pinene synthase (EC 4.2.3.14); or

(e) a monoterpene synthase.

10. The method of claim 2 wherein the enzymatic conversion of crotyl alcohol into crotyl phosphate is achieved by the use of a hydroxyethylthiazole kinase (EC 2.7.1.50) or a thiamine kinase (EC 2.7.1.89).

11. The method of claim 1 comprising the steps of

(I) enzymatically converting crotyl alcohol into crotyl diphosphate; and

(II) enzymatically converting crotyl diphosphate into butadiene.

12. The method of claim 11 wherein the enzymatic conversion of crotyl alcohol into crotyl diphosphate consists of a single enzymatic reaction in which crotyl alcohol is directly converted into crotyl diphosphate.

13. The method of claim 12 wherein the enzymatic conversion of crotyl alcohol into crotyl diphosphate is achieved by the use of a 2-amino-4-hydroxy-6-hydroxymethyldihydropteridine diphosphokinase (EC 2.7.6.3) or a thiamine diphosphokinase (EC 2.7.6.2).

14. The method of claims 11 wherein the enzymatic conversion of crotyl diphosphate into butadiene is achieved by the use of a terpene synthase.

15. The method of claim 14 wherein the terpene synthase is

(a) an isoprene synthase (EC 4.2.3.27); or

(b) a myrcene/ocimene synthase (EC 4.2.3.15); or

(c) a farnesene synthase (EC 4.2.3.46 or EC 4.2.3.47); or

(d) a pinene synthase (EC 4.2.3.14); or

(e) a monoterpene synthase.

16. The method of claim 1 further comprising the step of providing crotyl alcohol by the enzymatic conversion of crotonaldehyde into crotyl alcohol.

17. The method of claim 16 wherein the conversion of crotonaldehyde into crotyl alcohol is achieved by the use of

(i) a hydroxymethylglutaryl-CoA reductase (EC1.1.1.34); and/or

(ii) an alcohol dehydrogenase (EC 1.1.1.1); and/or

(iii) an aldehyde reductase; and/or

(iv) an aldo-keto reductase.

18. An organism or microorganism which expresses

A) (a) (i) a hydroxyethylthiazole kinase (EC 2.7.1.50); or (ii) a thiamine kinase (EC 2.7.1.89); and

 (b) (i) a terpene synthase; or (ii) an isopentenyl phosphate kinase and a terpene synthase; or

B) (a) (i) a 2-amino-4-hydroxy-6-hydroxymethyldihydropteridine diphosphokinase (EC 2.7.6.3); or (ii) a thiamine diphosphokinase (EC 2.7.6.2); and

 (b) a terpene synthase,

and which is capable of converting crotyl alcohol into butadiene.

19. A composition comprising the organism or microorganism of claim 18 and, optionally, crotyl alcohol.

20. A composition comprising:

A) (a) (i) a hydroxyethylthiazole kinase (EC 2.7.1.50); or (ii) a thiamine kinase (EC 2.7.1.89); and

 (b) (i) a terpene synthase; or (ii) an isopentenyl phosphate kinase and a terpene synthase; or

(B) (a) a 2-amino-4-hydroxy-6-hydroxymethyldihydropteridine diphosphokinase (EC 2.7.6.3); and

 (b) a terpene synthase.

21. The composition of claim 20 further comprising crotyl alcohol.

22. Use of a combination of enzymes comprising:

A) (a) (i) a hydroxyethylthiazole kinase (EC 2.7.1.50); or (ii) thiamine kinase (EC 2.7.1.89); and

 (b) (i) a terpene synthase; or (ii) an isopentenyl phosphate kinase and a terpene synthase; or

B) (a) a 2-amino-4-hydroxy-6-hydroxymethyldihydropteridine diphosphokinase EC 2.7.6.3); and

 (b) a terpene synthase;

for the production of butadiene from crotyl alcohol.

23. The organism of claim 18, wherein the terpene synthase is

(a) an isoprene synthase (EC 4.2.3.27); or

(b) a myrcene/ocimene synthase (EC 4.2.3.15); or

(c) a farnesene synthase (EC 4.2.3.46 or EC 4.2.3.47); or

(d) a pinene synthase (EC 4.2.3.14); or

(e) a monoterpene synthase.

24. A method for producing crotyl alcohol comprising the enzymatic conversion of crotonyl-CoA into crotonaldehyde and the subsequent enzymatic conversion of crotonaldehyde into crotyl alcohol.

25. The method of claim 24, wherein the enzymatic conversion of crotonyl-CoA into crotonaldehyde is achieved by the use of

(i) a hydroxymethylglutaryl-CoA reductase (EC 1.1.1.34); and/or

(ii) an acetaldehyde dehydrogenase (EC 1.2.1.10); and/or

(iii) an acyl-CoA reductase.

26. The method of claim 25 wherein the enzymatic conversion of crotonaldehyde into crotyl alcohol is achieved by the use of

(i) a hydroxymethylglutaryl-CoA reductase (EC 1.1.1.34); and/or

(ii) an alcohol dehydrogenase (EC 1.1.1.1); and/or

(iii) an aldehyde reductase; and/or

(iv) an aldo-keto reductase.

27. The method of claim 24 wherein the enzymatic conversion of crotonyl-CoA into crotyl alcohol is achieved by the use of an aldehyde/alcohol dehydrogenase or by the use of a hydroxymethylglutaryl-CoA reductase (EC 1.1.1.34) or by the use of a short-chain dehydrogenase/fatty acyl-CoA reductase.

28. The method of claim 1 further comprising the enzymatic conversion of crotonyl-CoA into crotyl alcohol.